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. 2,417 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,417 in last 12 months

Showing 1806118080 of 27,254 recalls

Medical DeviceDecember 16, 2016· Covidien LLC

Recalled Item: Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10 Recalled by Covidien...

The Issue: Labeling error: The label indicates the product is latex free, but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Cephalotin CE 256 Foam packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Imipenem IP32 Foam packaging Recalled by BioMerieux SA Due to Product...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Doripenem DOR32 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Ceftriaxone TXL32 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Benzyl Penicillin PG256 FOAM packaging Recalled by BioMerieux SA Due...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Vancomycin VA 256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Ceftazidime TZ256 Foam packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST¿ Ceftriaxone TXL32 SPB Recalled by BioMerieux SA Due to Product...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: Ciprofloxacin CI 32 Foam packaging Recalled by BioMerieux SA Due to Product...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Fosfomycin FM1024 Blister packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Tobramycin TM256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2016· BioMerieux SA

Recalled Item: ETEST Gentamicin GM256 FOAM packaging Recalled by BioMerieux SA Due to...

The Issue: Product Stability issues: The current shelf-life claims of the ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· Ultradent Products, Inc.

Recalled Item: NanoTips 30g 20pk Recalled by Ultradent Products, Inc. Due to Ultradent...

The Issue: Ultradent Products, Inc. announces a voluntary field action for the NanoTips...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· Organ Recovery Systems, Inc.

Recalled Item: SPS-1 Recalled by Organ Recovery Systems, Inc. Due to Organ preservation...

The Issue: Organ preservation fluid recalled due to potential for bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 16 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 12 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 14 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 16 mm [or 18 mm] Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2016· MEDLINE INDUSTRIES INC

Recalled Item: 10 mm Distraction Pin Recalled by MEDLINE INDUSTRIES INC Due to Product's...

The Issue: Product's non-conformity involves the integrity of the seal in the sterile...

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

Class II — Potential Health HazardOngoing