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EMERGENCY MEDICAL PRODUCTS

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Product Recall Information

It's hard to keep track of medical product recalls, so we've created an easy-to-access list for you. Below is a list of products we have distributed that have been effected by a notice of product recall or correction. If you have any questions, please contact customer service at (800) 824-6016 or email CustomerService@life-assist.com.

If you would like to be sent this list weekly, please sign-up here and select "Product Recalls" from the list of options.

Product Recalls
Date: 6/7/2017
Type: Urgent Product Recall
Manufacturer: Dukal
Product: Disposable Burn Sheet, Dukal Brand
LA Item No: BX7305
Manuf Item No: 7305
Reason: Dukal is recalling the Burn Sheets identified above based on a report of a Burn Sheet (stored for an unknown period of time and in unknown conditions) that was reportedly “shredded” when the outer package was opened. The lots listed were manufactured between 2007 and 2014.
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Lot Numbers: JT13607, JT17507, JT35207, JT09008, JT11308, JT15408, JT18408, JT18708, JT23408, JT24508, JT26408, JT28408, JT31408, JT33508, JT00609, JT04809, JT15209, JT18209, JT19209, JT22409, JT22709, JT23209, JT25309, JT25809, JT27509, JT30109, JT31309, JT32909, JT17510, JT23610, JT24010, JT24810, JT30810, JT35910, JT00811, JT05011, JT07911, JT11511, JT15911, JT17011, JT18211, JT21511, JT26311, JT28411, JT30711, JT00812, JT07312, JT11812, JT13612, JT17712, JT21812, JT25612, JT33012, JT36112, JT36212, JT09113, JT17513, JT24713, JT29813, JT33513, JT01614, JT04614, JT06814
Date: 4/28/2017
Type: Urgent: Drug Recall
Manufacturer: Hospiria
Product: Dextrose Infant 2.5 gm, 25%, 10 ml ANSYR™ Syringe
LA Item No: DR1775-01
Manuf Item No: 0409-1775-10
Reason: Hospira, Inc., a Pfizer company, is voluntarily recalling the item and lot referenced above, due to the presence of particulate matter, identified as human hair, found within an internal sample syringe.
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Lot Numbers: 58382EV (Lot may be followed by 01 or 02)
Date: 4/3/2017
Type: Urgent: Drug Recall
Manufacturer: Mylan
Product: EPIPEN Auto-Inject, 0.15 mg, Child, 2/PK
LA Item No: DR0501-02
Manuf Item No: 49502-0501-02
Reason: This recall is being conducted as a result of the receipt of two previously disclosed reports outside of the U.S. of failure to activate the device due to a potential defect in a supplier component.
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Lot Numbers: 5GM631, 5GM640, 6GM072, 6GM081, 6GM082, 6GM087, 6GM088, 6GM091, 6GM198, 6GM199, 6GN215, 5GN767, 5GN773
Date: 4/3/2017
Type: Urgent: Drug Recall
Manufacturer: Mylan
Product: EPIPEN Auto-Inject, 0.15 mg, Child, 2/PK (<12 mo exp date)
LA Item No: DR0501-02SD
Manuf Item No: 49502-0501-02
Reason: This recall is being conducted as a result of the receipt of two previously disclosed reports outside of the U.S. of failure to activate the device due to a potential defect in a supplier component.
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Lot Numbers: 5GM631, 5GM640, 6GM072, 6GM081, 6GM082, 6GM087, 6GM088, 6GM091, 6GM198, 6GM199, 6GN215, 5GN767, 5GN773
Date: 4/3/2017
Type: Urgent: Drug Recall
Manufacturer: Mylan
Product: EPIPEN Auto-Inject, 0.3 mg, Adult, 2/PK
LA Item No: DR0500-02
Manuf Item No: 49502-0500-02
Reason: This recall is being conducted as a result of the receipt of two previously disclosed reports outside of the U.S. of failure to activate the device due to a potential defect in a supplier component.
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Lot Numbers: 5GM631, 5GM640, 6GM072, 6GM081, 6GM082, 6GM087, 6GM088, 6GM091, 6GM198, 6GM199, 6GN215, 5GN767, 5GN773
Date: 4/3/2017
Type: Urgent: Drug Recall
Manufacturer: Mylan
Product: EPIPEN Auto-Inject, 0.3 mg, Adult, 2/PK (<12 mo exp date)
LA Item No: DR0500-02SD
Manuf Item No: 49502-0500-02
Reason: This recall is being conducted as a result of the receipt of two previously disclosed reports outside of the U.S. of failure to activate the device due to a potential defect in a supplier component.
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Lot Numbers: 5GM631, 5GM640, 6GM072, 6GM081, 6GM082, 6GM087, 6GM088, 6GM091, 6GM198, 6GM199, 6GN215, 5GN767, 5GN773
Date: 4/3/2017
Type: Urgent: Field Corrective Action Notice
Manufacturer: Medtronic
Product: Ventilator, HT70 with O2 monitor built in
LA Item No: TYCO_HT70PM-WW-NA
Manuf Item No: HT70PM-WW-NA
Reason: The ventilator may, on rare occasion, reset spontaneously during normal operations without an accompanying alarm.
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Lot Numbers: Newport HT70 and Newport HT70 Plus Ventilators
Date: 3/10/2017
Type: Urgent Medical Device Correction
Manufacturer: Philips Healthcare
Product: HeartStart MRx Monitor/Defibrillator
LA Item No: ED3536A
Manuf Item No: 861289
Reason: On exceptionally rare occasions units may exhibit abnormal behavior when operating using a single battery as the sole source of power. See attachment for more information.
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Lot Numbers: Philips HeartStart MRx Monitor/Defibrillator model numbers M3535A, M3536A, and military bundles.
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: CURITY® Eye Pad
LA Item No: BA2841
Manuf Item No: 2841
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Lot # beginning with 12, 13, 14, 15, 16
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: SALINE DRESSING, 4"X 8", CS/192
LA Item No: KEND_3606
Manuf Item No: 3606
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Lot # beginning with 14, 15, 16 (Excludes lots 16J098062, 16J098162, 16J098262)
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: SISKIYOU BURN KIT™
LA Item No: BU020A
Manuf Item No: 2841 Eye Pad ONLY
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Eye Pads within assemblages- Lot # beginning with 12, 13, 14, 15, 16
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: BURN FREE™ Burn Kit
LA Item No: BU030C
Manuf Item No: 2841 Eye Pad ONLY
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Eye Pads within assemblages- Lot # beginning with 12, 13, 14, 15, 16
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: Emergency First Aid Kit
LA Item No: FJ8000
Manuf Item No: 2841 Eye Pad ONLY
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Eye Pads within assemblages- Lot # beginning with 12, 13, 14, 15, 16
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: Responder II Kit™
LA Item No: KIT69
Manuf Item No: 2841 Eye Pad ONLY
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Eye Pads within assemblages- Lot # beginning with 12, 13, 14, 15, 16
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: Deluxe First Response Trauma Kit™, Orange
LA Item No: KIT77-ORG
Manuf Item No: 2841 Eye Pad ONLY
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Eye Pads within assemblages- Orange and Blue Kits - Lot # beginning with 12, 13, 14, 15, 16
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: KINGS™ Trauma Kit, Navy Blue
LA Item No: KIT4900-BLU
Manuf Item No: 2841 Eye Pad ONLY
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Eye Pads within assemblages- Red and Blue Kits - Lot # beginning with 12, 13, 14, 15, 16
Date: 3/9/2017
Type: Urgent Medical Device Recall
Manufacturer: Covidien
Product: First Response Trauma Kit™, Orange
LA Item No: KIT5025-ORG
Manuf Item No: 2841 Eye Pad ONLY
Reason: Medtronic is voluntarily recalling specific item codes and production lots of Covidien Curity™ & Kerlix™ products due to the potential for the sterile packaging to be compromised.
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Lot Numbers: Eye Pads within assemblages- Lot # beginning with 12, 13, 14, 15, 16
Date: 1/13/2017
Type: Urgent Device Recall
Manufacturer: Laerdal
Product: Laerdal™ Compact Suction Unit 800 ml (LCSU 4)
LA Item No: OK880051
Manuf Item No: 880051
Reason: Units may turn on spontaneously and/or may not turn off using the ‘On/Off’ button. This issue can occur while using the battery or external power
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Lot Numbers: Serial number range 150501A0001 to 161028A0XXX
Date: 1/13/2017
Type: Urgent Device Recall
Manufacturer: Laerdal
Product: Laerdal™ Compact Suction Unit 300 ml (LCSU 4)
LA Item No: OK880061
Manuf Item No: 880061
Reason: Units may turn on spontaneously and/or may not turn off using the ‘On/Off’ button. This issue can occur while using the battery or external power
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Lot Numbers: Serial number range 150501A0001 to 161028A0XXX
Date: 11/22/2016
Type: Urgent Drug Recall
Manufacturer: Hospira
Product: Fentanyl, 100mcg/2mL amp (BX/10)
LA Item No: SAS_DR9093-32
Manuf Item No: NDC #: 0409-9093-32
Reason: Hospira, Inc. is voluntarily recalling these lots due to confirmed complaints of ampules with broken tips.
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Lot Numbers: 59277EV, 60028EV, 60082EV (NOTE: These lot numbers may be followed by additional numbers from 01 to 99)
Date: 11/4/2016
Type: Urgent Device Recall
Manufacturer: Teleflex Medical
Product: MAD® Mucosal Atomization Device with 3cc Syringe
LA Item No: IT100
Manuf Item No: MAD100
Reason: Teleflex Medical is recalling these products as they may not deliver a fully atomized plume of medication. Teleflex Medical has received complaints that the affected lots produced a straight stream instead of an atomized spray.
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Lot Numbers: 160105, 160137, 160302, 160321, 160402, 160435, 160506, 160523, 160609, 160620, 160707, 160802, 160813
Date: 11/4/2016
Type: Urgent Device Recall
Manufacturer: Teleflex Medical
Product: MAD® Mucosal Atomization Device
LA Item No: IT103
Manuf Item No: MAD300
Reason: Teleflex Medical is recalling these products as they may not deliver a fully atomized plume of medication. Teleflex Medical has received complaints that the affected lots produced a straight stream instead of an atomized spray.
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Lot Numbers: 160108, 160117, 160126, 160145, 160146, 160200, 160219, 160225, 160231, 160300, 160313, 160327, 160400, 160409, 160422, 160432, 160440, 160500, 160518, 160602, 160611, 160621, 160631, 160701, 160708, 160718, 160728, 160800, 160804, 160814, 160816, 160823
Date: 11/4/2016
Type: Urgent Device Recall
Manufacturer: Teleflex Medical
Product: MAD® Mucosal Device with 3cc Syringe and Vial Adapter
LA Item No: IT140
Manuf Item No: MAD140
Reason: Teleflex Medical is recalling these products as they may not deliver a fully atomized plume of medication. Teleflex Medical has received complaints that the affected lots produced a straight stream instead of an atomized spray.
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Lot Numbers: 160125, 1602148, 160437, 160610, 160801
Date: 11/4/2016
Type: Urgent Device Recall
Manufacturer: Teleflex Medical
Product: MAD DEVICE W/1ML SYR & VIAL ACCESS, BX/25
LA Item No: RUSC_MAD130
Manuf Item No: MAD130
Reason: Teleflex Medical is recalling these products as they may not deliver a fully atomized plume of medication. Teleflex Medical has received complaints that the affected lots produced a straight stream instead of an atomized spray.
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Lot Numbers: 160107, 160138, 160517
Date: 9/15/2016
Type: Important Customer Nortice
Manufacturer: Motion Medical
Product: Emergency Cricothyrotomy Kit, 5.5mm
LA Item No: IVV1684
Manuf Item No: 1684-1
Reason: 1684-1 Cricothyrotomy Kit were delivered without the 4" Tracheal Hook
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Lot Numbers: Work order assembled on June 9th
Date: 9/15/2016
Type: Urgent Drug / Product Recall
Manufacturer: Major Pharmaceuticals
Product: Eye Wash, 4 oz.
LA Item No: MD537720
Manuf Item No: 301903 - NDC 0904-6491-20
Reason: Initiated due to potential microbial contamination
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Lot Numbers: G15905, G16902, G15906, G16903, G15907, G16905, G15910, G16906, G15911, G16907, G15912, , G16910, G16901, G16911
Date: 8/29/2016
Type: Urgent: Medical Device Correction
Manufacturer: Laerdal
Product: Laerdal™ LSU Suction Unit
LA Item No: OK7800
Manuf Item No: 78002001
Reason: Following storage at temperatures between 0°- 9°C (32°- 48°F), the LSU with NiMH Battery may shut off after a few seconds when operating at a vacuum level > ~200 mmHg when set to either the 350mmHg or 500+mmHg dial setting.
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Lot Numbers: All lot numbers sold between December 9, 2013 and July 26, 2016. Note: LSUs have been shipped with the NiMH Battery since December 9, 2013.
Date: 8/29/2016
Type: Urgent: Medical Device Correction
Manufacturer: Laerdal
Product: Laerdal™ LSU Suction Unit NiMH Battery
LA Item No: OK780800
Manuf Item No: 780800
Reason: Following storage at temperatures between 0°- 9°C (32°- 48°F), the LSU with NiMH Battery may shut off after a few seconds when operating at a vacuum level > ~200 mmHg when set to either the 350mmHg or 500+mmHg dial setting.
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Lot Numbers: All lot numbers sold between December 9, 2013 and July 26, 2016. Note: LSUs have been shipped with the NiMH Battery since December 9, 2013.
Date: 8/22/2016
Type: Label Revisions
Manufacturer: ConMed
Product: CONMED® PadPro™ Electrode, Physio Connector, Adult/Child
LA Item No: EL2001M
Manuf Item No: Adult
Reason: In an effort to maintain market consistency with AHA and keep pace with other defibrillator manufacturers.
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Lot Numbers: 2516 series, 2001 series, 2502 series (31 product codes)
Date: 8/22/2016
Type: Label Revisions
Manufacturer: ConMed
Product: CONMED® PadPro™ Electrode, Physio Connector, PEDI
LA Item No: EL2603M
Manuf Item No: Pediatric
Reason: In an effort to maintain market consistency with AHA and keep pace with other defibrillator manufacturers.
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Lot Numbers: 2603 series (7 product codes)
Date: 8/12/2016
Type: Urgent Recall
Manufacturer: C.R. Bard
Product: Toomey Syringe, 70cc
LA Item No: OK38
Manuf Item No: 0038460
Reason: Specific lot numbers may be at risk for having a slit defect on the packaging which could potentially compromise the product’s sterility.
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Lot Numbers: NGZC3768, NGZC5029, NGZD0924, NGZD1664, NGZD1983, NGZD3103, NGZD3241, NGZD3989, NGZD4053, NGZD4923, NGZE1190, NGZE2134, NGZE3406, NGZF0305, NGZF1546, NGZF2589, NGZF3934, NGZF4488, NGZF4885
Date: 7/7/2016
Type: Urgent Drug Recall
Manufacturer: Hospiria
Product: DIAZEPAM 10MG/2ML CARPUJECT LUER LOCK (BX/10)
LA Item No: DR1273-02
Manuf Item No: 0409-1273-32
Reason: Potential for the presence of crystallized Diazepam adhered to the plunger or wall of the Carpuject.
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Lot Numbers: 52610LL, 57660LL
Date: 7/7/2016
Type: Urgent Drug Recall
Manufacturer: Hospiria
Product: Diazepam, 10MG/2 ML, LL/CJ (BX/10)
LA Item No: PS_DR1273-32
Manuf Item No: 0409-1273-32
Reason: Potential for the presence of crystallized Diazepam adhered to the plunger or wall of the Carpuject.
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Lot Numbers: 52610LL, 57660LL
Date: 6/7/2016
Type: Urgent Drug Recall
Manufacturer: McKesson Packaging Services
Product: Aspirin, Children's Chewable, 81 mg (blister packs)
LA Item No: MD85281
Manuf Item No: 63739-434-01
Reason: This recall has been issued due to a mix up of secondary packaging labeling.
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Lot Numbers: 0110701
Date: 3/28/2016
Type: Market Withdrawal
Manufacturer: Hospiria
Product: Amidate, 40 mg, 20 ml LifeShield® Syringe
LA Item No: DR8060-29
Manuf Item No: 0409-8060-29
Reason: Potential for the product to not meet specification (OOS) prior to expiry.
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Lot Numbers: 42-257-DK, 49-426-DK, 51-394-DK, 53-228-DK
Date: 3/18/2016
Type: Urgent Voluntary Product Recall
Manufacturer: Becton Dickinson
Product: BD Angiocath™ AUTOGUARD™ IV Catheter, 24 GA x .75"
LA Item No: IT1700
Manuf Item No: 381700, 381720
Reason: The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage.
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Lot Numbers: Product Code 381700 - Lot #3121951, 3143801, 3190895, 3254585, 3303872, 4051735, 4133600, 4177944, 4219570, 4289603, 4317642, 5063833, 5106687, 5125665, 5230884, 5300771, 381720. Product Code 381720 - Lot # 3045792, 3106688, 3289840, 4059581, 4203557, 5002915, 5063827, 5125565, 5300772
Date: 11/9/2015
Type: Urgent Medical Device Recall
Manufacturer: Physio-Control
Product: PHYSIO-CONTROL EDGE Electrode with Preconnect, Adult
LA Item No: EL7017
Manuf Item No: 11996-000017
Reason: This voluntary recall is being conducted due to a low-level potential for damage to the wire insulation during the manufacturing process of these specific lots.
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Lot Numbers: 516907, 519815, 519816
Date: 11/4/2015
Type: Urgent Product Recall
Manufacturer: Masimo
Product: Rad-57™ Kit with SpCO and Adult Rainbow Sensor
LA Item No: PO3734
Manuf Item No: 2696
Reason: Masimo has identified specific LOTs of sensors that were manufactured with incompatible configurations. This could result in sensors that will either not provide readings for the SpCO and SpMet parameters or inaccurate readings. The specific behavior will depend on the firmware version of the technology board in the device.
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Lot Numbers: Box Lot #15JA8; Sensor Ref#-Lot# 24087-A15H754 or 24087-A15J726 or 24087-A15J824
Date: 10/15/2015
Type: Field Safety Notice – Medical Device Recall
Manufacturer: Sscor, Inc
Product: S-SCORT® Replacement DC Cable
LA Item No: OK80665
Manuf Item No: 80665
Reason: A user may encounter excessive resistance when plugging the input barrel of the 80665 DC charging cable into a device charging receptacle. SSCOR will be sending the Field Safety Notice and handling replacements directly with the customers.
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Lot Numbers: Devices manufactured and shipped with 80665 DC charging cable between 06/19/2015 and 08/27/2015
Date: 10/15/2015
Type: Field Safety Notice – Medical Device Recall
Manufacturer: Sscor, Inc
Product: S-SCORT® TEN Suction Unit
LA Item No: OK2100
Manuf Item No: 2100
Reason: A user may encounter excessive resistance when plugging the input barrel of the 80665 DC charging cable into a device charging receptacle. SSCOR will be sending the Field Safety Notice and handling replacements directly with the customers.
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Lot Numbers: AG4812, AG4813, AG4814, AG4815, AG4816, AG4820, AG4821, AG4822, AG4823, AG4824, AG4825
Date: 10/15/2015
Type: Field Safety Notice – Medical Device Recall
Manufacturer: Sscor, Inc
Product: S-SCORT® III Suction Unit
LA Item No: OK74000
Manuf Item No: 740000
Reason: A user may encounter excessive resistance when plugging the input barrel of the 80665 DC charging cable into a device charging receptacle. SSCOR will be sending the Field Safety Notice and handling replacements directly with the customers.
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Lot Numbers: 516013, 516014, 516015, 516016, 516017, 516033, 516034, 516035, 516036, 516037, 516124, 516125, 516126, 516127, 516243, 516244, 516245, 516246, 516294, 516295, 516296, 516297, 516298
Date: 10/15/2015
Type: Field Safety Notice – Medical Device Recall
Manufacturer: Sscor, Inc
Product: S-SCORT JR® QUICKDRAW #2400 Battery Powered Aspirator
LA Item No: OK2400
Manuf Item No: 2400
Reason: A user may encounter excessive resistance when plugging the input barrel of the 80665 DC charging cable into a device charging receptacle. SSCOR will be sending the Field Safety Notice and handling replacements directly with the customers.
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Lot Numbers: W05687
Date: 9/8/2015
Type: Urgent Recall
Manufacturer: Pyng Medical
Product: MATCombat Tourniquet, Olive/Black
LA Item No: TQ01
Manuf Item No: MATC
Reason: Some units may not be in the ready-to-use position out of the package and, therefore, could require resetting before applying to a patient.
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Lot Numbers: SL113171
Date: 9/8/2015
Type: Urgent Recall
Manufacturer: Pyng Medical
Product: MATResponder Tourniquet, Orange
LA Item No: TQ01-ORG
Manuf Item No: MATR
Reason: Some units may not be in the ready-to-use position out of the package and, therefore, could require resetting before applying to a patient.
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Lot Numbers: SL114711
Date: 8/27/2015
Type: Urgent Recall
Manufacturer: Nephron Pharmaceuticals
Product: Albuterol/Ipratropium (Generic DuoNeb), 3 ml (Box of 30)
LA Item No: DR0201-03
Manuf Item No: NDC 0487-0201-03
Reason: Identification of lubricant on the outer primary package during the manufacturing process.
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Lot Numbers: D4E20A
Date: 8/27/2015
Type: Urgent Recall
Manufacturer: Teleflex Medical Rüsch
Product: FLEXI-SLIP™ Stylette, 6 fr.
LA Item No: AC900-06A
Manuf Item No: 502501
Reason: Reports of the plastic coating of the stylet splitting and/or breaking off of the stylet.
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Lot Numbers: 12EE20, 12KE48, 14JG05, 12FE26, 13BG26, 14JE43, 12GE27, 13BG36, 14KG27, 12IE37, 13DG24, 14LG06, 12GE30, 14FG03, 15BG05, 13AG21, 14GG01, 15AG34, 12LG29, 14GG03, 15AG28, 12IE36, 14HE32, 15CG24, 12IE39, 14HE34, 15DE18, 13DG06, 14IE36, 15DG38, 12JE41, 14KG11, 15EG08
Date: 7/13/2015
Type: Urgent Medical Device Correction
Manufacturer: Covidien
Product: Nellcor® OxiMax® N-65 Pulse Oximeter
LA Item No: PO65
Manuf Item No: N65-NA1
Reason: Customers have reported that Nellcor™ N-65 Handheld Pulse Oximeters and N-560 Pulse Oximeters do not fully display segments of numeric data, which may lead to an end user's misinterpretation of the numeric data being displayed.
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Lot Numbers: All Lots
Date: 7/2/2015
Type: Urgent Recall
Manufacturer: O-Two
Product: O-Two CPR Ventilation Timing Light, ADULT
LA Item No: OM1000TL
Manuf Item No: 01BM1000-CS
Reason: The flash rate of the malfunctioning device was reported to be twice that of the rate noted on the label.
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Lot Numbers: 079810
Date: 7/2/2015
Type: Urgent Recall
Manufacturer: O-Two
Product: BVM, SMART BAG ADULT W/ TIMING LIGHT, CS/12
LA Item No: OTWO_01BM3201MOTLCS
Manuf Item No: 01BM3201-MO-TL-CS
Reason: The flash rate of the malfunctioning device was reported to be twice that of the rate noted on the label.
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Lot Numbers: 140719, 140506
Date: 4/7/2015
Type: Urgent Recall
Manufacturer: Cooper Surgical
Product: TransWarmer® Infant Mattress
LA Item No: DI421
Manuf Item No: 20421
Reason: Serious burns have been reported in the past and could occur if the products are not stored under the labeled
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Lot Numbers: Any without Lot # or Expiration Date
Date: 3/31/2015
Type: Urgent Recall
Manufacturer: Baxter
Product: Baxter IV Solution, Dextrose 10%, 250 ml Bag
LA Item No: BAXT_2B0162QEA
Manuf Item No: 2B0162Q
Reason: Potential presence of particulate matter
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Lot Numbers: C965558, C963520
Date: 1/22/2015
Type: Urgent Recall
Manufacturer: Teleflex Medical
Product: Aquapak® Humidifier, Pre-filled, 340 mL
LA Item No: OH0340
Manuf Item No: 003-40
Reason: Packages may contain foreign material (black particles)
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Lot Numbers: 062137, 030137, 038137, 039137, 054137, 088137, 445147, 052137, 051137, 380137, 055137, 167137, 176137, 271147, 356147, 585137, 260147, 625137, 131137, 113147, 279137, 281137, 083137, 285147, 090147, 295147, 374137, 621137, 387147, 093137, 404147, 088147, 333147, 059147, 058137, 120137, 374147, 484137, 642137, 249147, 323137 407147, 605137, 293147, 294137, 639137, 166137, 306147, 264147, 138147, 604137, 034147, 536137, 271137, 099137, 190137, 371137, 369137, 137147, 225147, 239137, 651137 ,239137, 550137, 517137, 401147, 004147, 064137, 127137, 386147, 056137, 100137, 157137, 224147, 398147, 365147, 129137, 248147, 622137, 183147, 265137, 351137, 275147, 258137, 432137, 158147, 283137, 399147, 074147, 405147, 262137, 095137, 201137, 252137, 571137, 155147, 112137, 114137, 359137, 308147, 280137, 050147, 141137, 599137, 139147, 156147, 177137, 630137, 261147, 373147, 497137, 544139, 274147, 383147, 359147, 097147, 172147, 212147, 188137, 371147, 097137, 288147, 289137, 541137, 247137, 157147, 421137, 345137, 154137, 272137, 284137, 266147, 085137, 342147, 195137, 205137, 253137, 170137, 102137, 135137, 272147, 184147, 171137, 095147, 311147, 617137, 043137, 136137, 458137, 581137, 435137, 222147, 349147, 403147, 173137, 054147, 400147, 235137, 320137, 450137, 306137, 640137, 218147, 441137, 405137, 109137, 573137, 111137, 274137, 434137, 576137, 510137, 117137, 375137, 246147, 243147, 238147, 373137, 602137, 208147, 232147, 081147, 273137, 276137, 439137, 440137, 648137, 268147, 110137, 270147, 561137, 215147, 278137, 089137, 555137, 140137, 557137, 559137, 060147, 148137, 131147, 461137, 460137, 446137, 185147, 255147, 071147, 442147, 077137, 164137, 449137, 087137, 152137, 106147, 304147, 482137, 037147, 075137, 217147, 382147, 289147, 495137, 045137, 459137, 302147, 377147, 180147, 537137, 209147, 119137, 110147, 126147, 132137, 162137, 319137, 016147, 628137, 179147, 583137, 308137, 084147, 343147, 445137, 237147, 070147, 241147, 514137, 229147, 089147, 028147, 219147, 031147, 080147, 273147, 377137, 277137, 296147, 341147, 331147, 526137, 394147, 340147, 072137, 254137, 402147, 457137, 379147, 577137, 649137, 067137, 520137, 220147, 368137, 543137, 376137, 586137, 107147, 216147, 388147, 226137, 108137, 304137, 242147, 134147, 090137, 348147, 384147, 239147, 455137 ,513137, 456137, 593137, 048147, 079147, 094147, 098137, 240147, 603137, 251137, 522137, 498137, 529137, 159147, 315147, 376147, 050137, 392147, 085147, 438137, 168137, 341137, 339147, 048137, 443137, 224137, 064147, 368147, 073137, 442137, 056147, 138137, 043147, 290147, 397147, 358137, 338147, 150137, 503137, 123147, 507137, 204137, 300147, 071137, 291147, 221147, 314147, 312147
Date: 1/22/2015
Type: Urgent Recall
Manufacturer: Teleflex Medical
Product: Aquapak® Humidifier, Pre-filled, 650 mL
LA Item No: OH0640
Manuf Item No: 006-40
Reason: Packages may contain foreign material (black particles)
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Lot Numbers: 033137, 030136, 028136, 026136, 042146, 061146, 125136, 061136, 038147, 139136, 024136, 101136, 135136, 173136, 198136, 067136, 192136, 177136, 059136, 022146, 067146, 119136, 034136, 045146, 152136, 157136, 042136, 053136, 051146, 100136, 145136, 045136, 137136, 047136, 182136, 176136, 154136, 172136, 131136, 138136, 191136, 021146, 1901136, 098136, 050146, 156136, 185136, 043136, 096136, 189136, 150136, 044136, 155136, 181136, 184136, 043146, 196136, 144136, 136136, 183136, 072136, 188136, 197136, 049146, 099136, 073136, 151136, 041136, 071136, 064146, 065146, 064136, 063136, 066136, 060146, 058136, 065136, 186136, 025136, 097136, 124136, 046136, 044146, 066146
Date: 1/22/2015
Type: Urgent Recall
Manufacturer: Hospiria
Product: Ketorolac, 30 mg, 1 ml, VIAL
LA Item No: DR3795-01
Manuf Item No: 3795-01
Reason: Potential for particulate
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Lot Numbers: 25-047-DK, 25-048-DK, 26-151-DK, 28-059-DK, 28-071-DK, 28-072-DK, 28-479-DK, 28-480-DK, 29-556-DK, 29-557-DK, 35-232-DK, 35-233-DK, 35-234-DK, 35-501-DK, 36-341-DK, 36-342-DK, 36-343-DK, 36-353-DK, 36-429-DK, 36-430-DK, 37-141-DK, 37-142-DK, 37-144-DK, 37-145-DK, 37-353-DK, 38-141-DK, 38-143-DK, 39-014-DK, 39-104-DK, 40-301-DK, 40-536-DK, 40-537-DK, 40-544-DK, 40-548-DK, 41-078-DK, 42-207-DK, 42-253-DK, 45-358-DK, 45-359-DK, 46-043-DK, 46-044-DK, 46-047-DK
Date: 1/21/2015
Type: Urgent Recall
Manufacturer: Hospiria
Product: Sodium Chloride IV Solution, 0.9%, Hospira, 250 ml Bag
LA Item No: SL7983-02
Manuf Item No: 7983-02
Reason: Report of particulate
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Lot Numbers: 44-002-JT
Date: 11/5/2014
Type: Urgent Recall
Manufacturer: Carefusion
Product: SCRUB BRUSH, 4% CHG, BX/30
LA Item No: MEDL_CFN4458AZ
Manuf Item No: CFN4458AZ
Reason: Higher concentrations of available CHG than what is stated on the product labeling.
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Lot Numbers: All Lots
Date: 11/5/2014
Type: Urgent Recall
Manufacturer: Carefusion
Product: SCRUB BRUSH, EZ SCRUB 4% CHG, BX/30
LA Item No: PHS_371073
Manuf Item No: CFN4458AZ
Reason: Higher concentrations of available CHG than what is stated on the product labeling.
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Lot Numbers: All Lots
Date: 10/17/2014
Type: Urgent Recall
Manufacturer: Hospiria
Product: Lactated Ringers IV Solution, Hospira, 1000 ml Bag
LA Item No: SL7953-09
Manuf Item No: 7953-09
Reason: Potential for leakage in flexible containers containing intravenous solutions
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Lot Numbers: 32-099-JT, 32-103-JT, 34-070-JT, 34-086-JT, 34-165-JT, 35-085-JT, 35-115-JT, 35-121-JT, 36-057-JT
Date: 10/17/2014
Type: Urgent Recall
Manufacturer: Hospiria
Product: Sodium Chloride IV Solution, 0.9%, Hospira, 1000 ml Bag
LA Item No: SL7983-09
Manuf Item No: 7983-09
Reason: Potential for leakage in flexible containers containing intravenous solutions
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Lot Numbers: 32-044-JT, 32-072-JT, 32-102-JT, 33-028-JT, 33-046-JT, 33-049-JT, 33-061-JT, 33-085-JT, 33-096-JT, 33-101-JT, 33-102-JT, 34-016-JT, 34-085-JT, 34-122-JT, 34-123-JT, 35-026-JT, 35-030-JT, 35-067-JT, 36-002-JT, 36-029-JT, 36-049-JT, 36-058-JT, 36-103-JT, 37-013-JT
Date: 7/28/2014
Type: Urgent Recall
Manufacturer: Baxter
Product: Baxter INTERLINK® Buretrol® IV Set
LA Item No: IV2C7564
Manuf Item No: 2C7564
Reason: Possible separation between burette chamber and drip chamber
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Lot Numbers: DR13E06019, DR13I16010, DR13J03033, DR13J09014, DR13K07024, DR13K18021, DR13L02023, DR13L18011, DR14A10035, DR14A30017, DR14B11023, DR14B20016, DR14B26039, DR13E07017, DR13I16028, DR13J04015, DR13J09022, DR13K08022, DR13K19029, DR13L03039, DR13L18029, DR14A23012, DR14B06049, DR14B13037, DR14B20032, DR14C05015, DR13E07025, DR13I23016, DR13J04023, DR13J24021, DR13K12024, DR13K25026, DR13L10018, DR13L19035, DR14A23020, DR14B07013, DR14B13045, DR14B21014, DR14C05031, DR13I14023, DR13I23024, DR13J08024, DR13J24039, DR13K13022, DR13K26024, DR13L11016, DR14A09052, DR14A29027, DR14B07047, DR14B14019, DR14B26013
Date: 7/28/2014
Type: Urgent Recall
Manufacturer: Baxter
Product: Baxter CLEARLINK® Buretrol® IV Set
LA Item No: IV2C8864
Manuf Item No: 2C8864
Reason: Possible separation between burette chamber and drip chamber
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Lot Numbers: DR13E08015, DR13E08023, DR13E09013, DR13I26027, DR13I27017, DR13I27025, DR13I28015, DR13I28023, DR13J16027, DR13J17025, DR13J28022, DR13J29020, DR13K01019, DR13K20027, DR13K21025, DR13L19019, DR13L19027, DR14A11017, DR14A14011, DR14A24010, DR14A24036, DR14A31049, DR14B07054, DR14B22012, DR14B28050, DR14C01030, DR14C06013, DR14C069039