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. 2,348 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,348 in last 12 months

Showing 2534125360 of 46,762 recalls

Medical DeviceJanuary 30, 2018· Encore Medical, Lp

Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: Broken or missing screws and retaining clips. This may be due to screw...

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

Class II — Potential Health HazardOngoing
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 40 mg Recalled by Dr. Reddy's Laboratories,...

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

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 25 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Mckesson Packaging Services

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Packaging Services...

The Issue: Subpotent Drug: Out of specification for assay (stability testing)

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 75 mcg/h Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 10 mg Recalled by Dr. Reddy's Laboratories,...

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

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

Class III — Low RiskOngoing
Refund
DrugJanuary 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 20 mg Recalled by Dr. Reddy's Laboratories,...

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

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 29, 2018· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...

The Issue: The device may process the same sample with two different sample IDs and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack: 1) UDI-M535SAK3010 Recalled by NxStage Medical, Inc....

The Issue: May contain endotoxin levels which have been confirmed to exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Stryker Communications

Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...

The Issue: The device could have a missing spanner nut and snap ring which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Philips Electronics North America Corporation

Recalled Item: Philips QCPR Meter - used with FR3 Product Usage: The Recalled by Philips...

The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Philips Electronics North America Corporation

Recalled Item: Philips QCPR Meter - used with MRx Product Usage: The Recalled by Philips...

The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...

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

Class II — Potential Health HazardOngoing
DrugJanuary 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel (flavocoxid 500 mg) capsules Recalled by Primus Pharmaceuticals,...

The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...

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

Class I — Serious Health HazardOngoing
Refund