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. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 3904139060 of 46,762 recalls

Medical DeviceJuly 25, 2014· Estill Medical Technologies, Inc

Recalled Item: Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery...

The Issue: Estill has discovered that a fully discharged Ultra Battery 1 (TA-UB1) will...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· JK Products & Services, Inc

Recalled Item: SUN DASH RADIUS 252 PN 8000809705. The device is intended Recalled by JK...

The Issue: The integrity of the wires inside main electrical chord become compromised...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2014· OrthoPediatrics Corp

Recalled Item: ACL Sleeve Installation Tool Sizes: 6mm Recalled by OrthoPediatrics Corp Due...

The Issue: Weld fractures on the Sleeve Installation Tool for ACL reconstruction system.

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

Class II — Potential Health HazardOngoing
DrugJuly 25, 2014· Sandoz Incorporated

Recalled Item: Alprazolam Tablets Recalled by Sandoz Incorporated Due to Presence of...

The Issue: Presence of Foreign Substance; tablets may contain stainless steel metal...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Fagron, Inc

Recalled Item: Fagron Recalled by Fagron, Inc Due to Microbial Contamination of Non-Sterile...

The Issue: Microbial Contamination of Non-Sterile Products: Fagron is recalling six...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Wockhardt Usa Inc.

Recalled Item: Wockhardt Metoprolol Succinate Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: Dissolution failures found during testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Fagron, Inc

Recalled Item: Fagron Recalled by Fagron, Inc Due to Microbial Contamination of Non-Sterile...

The Issue: Microbial Contamination of Non-Sterile Products: Fagron is recalling six...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 24, 2014· Fagron, Inc

Recalled Item: Fagron Recalled by Fagron, Inc Due to Microbial Contamination of Non-Sterile...

The Issue: Microbial Contamination of Non-Sterile Products: Fagron is recalling six...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2014· GoMacro, Inc.

Recalled Item: gomacro MACROBAR brand almond butter + carob. Net Wt. 2 oz (57 g) Recalled...

The Issue: GoMacro is recalling MARCO BARS brand almond butter + carob (lots 1634 and...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 24, 2014· GoMacro, Inc.

Recalled Item: gomacro MACROBAR brand sunflower butter + chocolate Net Wt. 2.3 oz (65 g)...

The Issue: GoMacro is recalling MARCO BARS brand almond butter + carob (lots 1634 and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 24, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker T2 Tibia System Nail Insertion Sleeve Recalled by Stryker Howmedica...

The Issue: Stryker Orthopaedics received a report indicating some of the Nail Insertion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Vl DBL OFFST WI LRG STPL Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 D8L OFFSET RASP HANDLE Recalled by Zimmer, Inc. Due to The firm...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: Double Offset Rasp Handle Recalled by Zimmer, Inc. Due to The firm received...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: VER2 HANDLE Recalled by Zimmer, Inc. Due to The firm received complaints for...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2014· Zimmer, Inc.

Recalled Item: 23.5 Deg Rasp Handle Assy- LEFT Nonsterile Recalled by Zimmer, Inc. Due to...

The Issue: The firm received complaints for failure of the handle to remain assembled...

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

Class II — Potential Health HazardOngoing