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 1376113780 of 46,762 recalls

DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide...

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2021· Beiersdorf Inc

Recalled Item: Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...

The Issue: Chemical contamination; presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2021· Mentor Texas, LP.

Recalled Item: MENTOR Saline-Filled Breast Implants are constructed from room temperature...

The Issue: Due to a manufacturing issue, Implant may have a potentially weakened area...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· Abbott Laboratories

Recalled Item: ARCHITECT i1000SR /1L86 and 1L87 Recalled by Abbott Laboratories Due to...

The Issue: Twelve software-related issues affecting software version 9.41 and earlier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· Abbott Laboratories

Recalled Item: ARCHITECT c4000 /2P24 Recalled by Abbott Laboratories Due to Twelve...

The Issue: Twelve software-related issues affecting software version 9.41 and earlier...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· CooperSurgical, Inc.

Recalled Item: LEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120...

The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2021· Baxter Healthcare Corporation

Recalled Item: Hemodialysis Delivery System Recalled by Baxter Healthcare Corporation Due...

The Issue: If the operator initiates therapy with a saved prescription profile and...

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2021· Revive Personal Products Company

Recalled Item: The Natural Dentist Healthy Balance Peppermint Sage Recalled by Revive...

The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 28, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...

The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2021· Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...

The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2021· Strides Pharma Inc.

Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by Strides Pharma Inc....

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2021· AMIVAS (US), LLC

Recalled Item: Artesunate for Injection Recalled by AMIVAS (US), LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Air filter failed post integrity test...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2021· O&M HALYARD INC

Recalled Item: HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES Recalled by O&M...

The Issue: All lots of the glove may discolor and lose elasticity upon aging, resulting...

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

Class II — Potential Health HazardOngoing