Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1586115880 of 46,762 recalls

DrugDecember 23, 2020· Genus Lifesciences Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Genus Lifesciences Inc....

The Issue: Presence of Foreign Substance: Particulate matter was found in multiple lots...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Recalled by...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Valkyrie LTOWB Collection (P/N 80-820 Recalled by Combat Medical Systems,...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Recalled...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN Recalled by Combat...

The Issue: There is the potential of a bent or disconnected needle in one of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Becton Dickinson & Company

Recalled Item: BD Hypodermic Syringe 10 ml Recalled by Becton Dickinson & Company Due to...

The Issue: The product packaging for the 10 ml eccentric tip syringe may exhibit open...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2020· Draegar Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution: The IACS is Recalled...

The Issue: The Infinity M540 patient monitor may randomly reboot due to an error to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2020· Biomet, Inc.

Recalled Item: A.L.P.S. Clavicle Plating System Recalled by Biomet, Inc. Due to The...

The Issue: The instruments may become cold welded together when the drill is inserted...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2020· EOS Imaging

Recalled Item: The EOSedge system may acquire two simultaneous orthogonal planar images...

The Issue: Inadequate images resizing and 2D measurement errors may occur when biplanar...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used Recalled by...

The Issue: FUJIFILM has become aware that incorrect concentration values were printed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 22, 2020· Abbott Point Of Care Inc.

Recalled Item: Abbott i-STAT CG8+ cartridges - IVD Intended for quantitative measurement...

The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2020· Abbott Point Of Care Inc.

Recalled Item: Abbott i-STAT EG7+ cartridge-IVD. Intended for the quantitative measurement...

The Issue: Ionized calcium test on some i-STAT CG8+ and EG7+ cartridges may exhibit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 21, 2020· Merck Sharp & Dohme

Recalled Item: Zerbaxa (ceftolozane and tazobactam) 1.5g per vial for injection Recalled by...

The Issue: Lack of assurance of sterility: The results of sterility tests of seven...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 21, 2020· Getinge Group Logistics America, LLC

Recalled Item: Getinge CM320 Series Washer Disinfector - Product Usage: A multi Recalled by...

The Issue: The potential that the plastic inlet hose connections may deform or break as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2020· Baxter Healthcare Corporation

Recalled Item: Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set Recalled by...

The Issue: There were customer reports of separation between the tubing and Male Luer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2020· Nihon Kohden America Inc

Recalled Item: PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No....

The Issue: Medical device non-conformance to electrical safety standard (IEC 60601-1).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2020· Smiths Medical ASD Inc.

Recalled Item: Portex Acapella DH Vibratory PEP Device - Product Usage: a Recalled by...

The Issue: Shipping box may contain wrong model.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 18, 2020· KVK-Tech, Inc.

Recalled Item: Benzhydrocodone and Acetaminophen Tablets Recalled by KVK-Tech, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; out of specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 18, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...

The Issue: Misleading error messages and a gap in the Operator Manual which affects...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing