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. 2,326 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,326 in last 12 months

Showing 3384133860 of 46,762 recalls

FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: Colostrum Lozenges Recalled by Immuno - Dynamics, Inc Due to The PerCoBa...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: Colostrum Powder Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa 1 Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand and...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa Colostrum Capsules Recalled by Immuno - Dynamics, Inc Due to The...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa Whey Protein Isolate with Colostrum Recalled by Immuno - Dynamics,...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension EXL with LM STM Product Recalled...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension RxL Max w/o HM Product Recalled by...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension EXL with LM Product Usage:...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· C.R. Bard, Inc.

Recalled Item: Arctic Sun 5000 and Arctic Sun 2000 Recalled by C.R. Bard, Inc. Due to...

The Issue: Improper targeted temperature therapy was delivered to patients because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Philips Healthcare

Recalled Item: Philips Healthcare DigitalDiagnost stationary X-ray system Recalled by...

The Issue: The detector may signal that it is ready for acquisition when it actually is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Aesculap, Inc.

Recalled Item: Flexible Drill Recalled by Aesculap, Inc. Due to The flexible shaft of the...

The Issue: The flexible shaft of the instruments may break during orthopedic spinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Aesculap, Inc.

Recalled Item: Flexible Screw Driver SJ706R Recalled by Aesculap, Inc. Due to The flexible...

The Issue: The flexible shaft of the instruments may break during orthopedic spinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Aesculap, Inc.

Recalled Item: Tray Set containing multiple instruments and may contain the flexible bone...

The Issue: The flexible shaft of the instruments may break during orthopedic spinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Aesculap, Inc.

Recalled Item: Flexible Bone Awl Recalled by Aesculap, Inc. Due to The flexible shaft of...

The Issue: The flexible shaft of the instruments may break during orthopedic spinal...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension RxL Max HM STM Product Recalled by...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Philips Healthcare

Recalled Item: Philips Healthcare DuraDiagnost stationary X-ray system Recalled by Philips...

The Issue: The detector may signal that it is ready for acquisition when it actually is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2015· Medtronic Inc.

Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...

The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2015· C.R. Bard, Inc.

Recalled Item: Arctic Sun Temperature Management System Recalled by C.R. Bard, Inc. Due to...

The Issue: The product may contain electronic components that lead to a premature...

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

Class II — Potential Health HazardOngoing
DrugNovember 9, 2015· Freedom Pharmaceuticals Inc

Recalled Item: Baclofen USP powder Recalled by Freedom Pharmaceuticals Inc Due to Presence...

The Issue: Presence of Foreign Substance

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2015· Zenobia Co.

Recalled Item: My Spice Sage Ground Flax Seed Meal under the following Recalled by Zenobia...

The Issue: Zenobia Company, LLC is recalling Flax Seed Meal due to the possible...

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

Class I — Serious Health HazardOngoing
Refund