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. 2,336 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,336 in last 12 months

Showing 2998130000 of 46,762 recalls

DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Indiomin MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2016· Domain Surgical, Inc.

Recalled Item: FMsealer Open Shears. Model FM3001 Recalled by Domain Surgical, Inc. Due to...

The Issue: Domain Surgical, Inc. announces a voluntary field action for the FMsealer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2016· Beckman Coulter Inc.

Recalled Item: Access Ostase Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2016· Beckman Coulter Inc.

Recalled Item: Access Ostase QC Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2016· Akorn Inc

Recalled Item: Sodium Chloride Ophthalmic Solution Recalled by Akorn Inc Due to Subpotent...

The Issue: Subpotent Drug: concentration of product is less than labeled amount.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2016· Centurion Medical Products Corporation

Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...

The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Recovery of Incorrect Isocenter -operational change

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

Class II — Potential Health HazardOngoing
DrugOctober 20, 2016· CutisPharma, Inc.

Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...

The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...

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

Class III — Low RiskOngoing
Refund
DrugOctober 20, 2016· CutisPharma, Inc.

Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...

The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...

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

Class III — Low RiskOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Michigan Cherry Preserves 12oz glass bottles and 1 Recalled...

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass bottles Recalled...

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms America's Original Cherry Butter 12oz and 22oz glass...

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Strawberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 20, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Cherry Raspberry Preserves 12oz glass bottles and 1 gallon....

The Issue: Products contain milk not declared on the label.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 20, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens is providing software update version VA50A_SP3 to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...

The Issue: A product issues happens for RF projection images. If user measures on RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2016· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...

The Issue: Software defect:2D projection of contours in Verity. The defect causes...

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

Class II — Potential Health HazardOngoing
DrugOctober 19, 2016· Janssen Ortho L.L.C.

Recalled Item: Invokamet (canagliflozin and metformin HCl) tablets Recalled by Janssen...

The Issue: Labeling: Incorrect or Missing Package Insert - Xarelto prescribing...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 19, 2016· Greatbatch Medical

Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...

The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...

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

Class II — Potential Health HazardOngoing