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. 2,503 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,503 in last 12 months

Showing 1200112020 of 46,762 recalls

DrugApril 25, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Zonisamide Capsules USP Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Zonisamide Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 25, 2022· GE Healthcare, LLC

Recalled Item: Back up batteries in Avance CS2 and Avance CS2 Pro Recalled by GE...

The Issue: Backup batteries can fail earlier than their estimated life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2022· GE Healthcare, LLC

Recalled Item: Field replacement back up batteries distributed on or after April 1 Recalled...

The Issue: Backup batteries can fail earlier than their estimated life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2022· CardioTek BV

Recalled Item: CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device...

The Issue: Device did not pass electrical safety testing for adequate insulation.

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

Class II — Potential Health HazardOngoing
DrugApril 22, 2022· Pfizer Inc.

Recalled Item: Accupril (Quinapril HCl Tablets) 10 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2022· Pfizer Inc.

Recalled Item: Accupril (Quinapril HCl Tablets) 20 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2022· Pfizer Inc.

Recalled Item: Accupril (Quinapril HCl Tablets) 40 mg Recalled by Pfizer Inc. Due to CGMP...

The Issue: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Start-up time for the flow rate range greater than 50 ml/hr, and less than...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2022· Ivenix, Inc.

Recalled Item: Ivenix Infusion System (IIS) Recalled by Ivenix, Inc. Due to Downstream...

The Issue: Downstream occlusion alarm is sometimes immediately followed by a pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2022· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper...

The Issue: Part (A-rubber) intended for a different model of gastrointestinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2022· Olympus Corporation of the Americas

Recalled Item: Colonovideoscope Model CF-H180AL Recalled by Olympus Corporation of the...

The Issue: A (Camera unit) CCD intended for a different model of colonoscope may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2022· Bard Peripheral Vascular Inc

Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to There is the potential that...

The Issue: There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2022· Steris Corporation

Recalled Item: Reliance Synergy Washer/Disinfector Recalled by Steris Corporation Due to...

The Issue: The firm identified that when the electrical contactor component in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2022· ConvaTec, Inc

Recalled Item: SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market Recalled...

The Issue: Firm received 10 complaints of skin barrier delamination issues (e.g. flange...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2022· Smith & Nephew Orthopaedics GmbH

Recalled Item: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 Recalled by Smith &...

The Issue: Right nails were anodized, marked, and labelled as left nails and vice versa

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

Class II — Potential Health HazardOngoing
DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Erythromycin Topical Gel USP Recalled by McKesson Corporation dba McKesson...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Halobetasol Propionate Ointment 0.05% Net Wt. Recalled by McKesson...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Lidocaine Prilocaine Cream USP Recalled by McKesson Corporation dba McKesson...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund