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. 2,374 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,374 in last 12 months

Showing 2284122860 of 46,762 recalls

FoodSeptember 21, 2018· Victoria Gourmet, Inc.

Recalled Item: Victoria Taylor's Seasonings - Blackening Rub Recalled by Victoria Gourmet,...

The Issue: Product labeling is incorrect.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 20, 2018· Micro-Tech (Nanjing) Co., Ltd.

Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...

The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2018· AS Software, Inc.

Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....

The Issue: Any change made to current ultrasound machine software or hardware upgrades,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing
DrugSeptember 20, 2018· Pfizer Inc.

Recalled Item: Meropenem for Injection Recalled by Pfizer Inc. Due to Lack of assurance of...

The Issue: Lack of assurance of sterility: loss of container integrity.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2018· Pfizer Inc.

Recalled Item: Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle...

The Issue: CGMP Deviations; rejected product was used to manufacture final bulk lot

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2018· Pfizer Inc.

Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...

The Issue: Lack of assurance of sterility -Reports of loose metal ferrule crimps on...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2018· Upsher Smith Laboratories, Inc.

Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/ degradation specifications: Product is Out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2018· Upsher Smith Laboratories, Inc.

Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/ degradation specifications: Product is Out of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...

The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2018· Beckman Coulter Inc.

Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...

The Issue: Cross contamination may have occurred between wells for the reagent pack. As...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2018· COVIDIEN LLC

Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...

The Issue: Software Update: External USB Drive performance and its impact on Graphic...

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

Class I — Serious Health HazardOngoing
DrugSeptember 18, 2018· Xiromed LLC

Recalled Item: Altavera Levonorgestrel and Ethinyl Estradiol Tablets Recalled by Xiromed...

The Issue: Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 17, 2018· Endo Pharmaceuticals, Inc.

Recalled Item: robaxin-750 (methocarbamol tablets Recalled by Endo Pharmaceuticals, Inc....

The Issue: Labeling: Incorrect Instructions: Dosage information on the immediate...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 17, 2018· Medline Industries Inc

Recalled Item: SparkleFresh Fluoride Toothpaste Recalled by Medline Industries Inc Due to...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2018· Otsuka Pharmaceutical Development & Commercialization, Inc.

Recalled Item: treatNOW ABILIFY (aripiprazole) / ABILIFY MAINTENA 400-mg (aripiprazole) for...

The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 17, 2018· Otsuka Pharmaceutical Development & Commercialization, Inc.

Recalled Item: treatNOW ABILIFY (aripiprazole) and ABILIFY MAINTENA (aripiprazole) 400MG...

The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 17, 2018· BioMerieux SA

Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...

The Issue: Data loggers showed that one shipment to the United States experienced low...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Sterilmed, Inc.

Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...

The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...

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

Class II — Potential Health HazardOngoing