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. 2,283 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,283 in last 12 months

Showing 4142141440 of 46,762 recalls

Medical DeviceOctober 1, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Cancellous Bone Screw Howmedica Osteonics Corp. Stryker...

The Issue: Stryker received a report from the field indicating that a 5.5 mm Cancellous...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2013· Helix Medical LLC

Recalled Item: Blom-Singer Adjustable Tracheostoma Valve II Models: BE8025H and BE8025H-R3...

The Issue: InHealth Technologies (IHT) is recalling the Blom-Singer Adjustable...

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

Class III — Low RiskOngoing
DrugSeptember 30, 2013· G & W Laboratories Inc

Recalled Item: G & W Fluocinolone Acetonide Cream USP 0.025% Recalled by G & W Laboratories...

The Issue: Failed Content Uniformity Specifications; at the 18 month time point.

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 30, 2013· Merit Medical Systems, Inc.

Recalled Item: Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine...

The Issue: Custom Procedural Trays/Kits contain 1% Lidocaine HCl injection which were...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Recalled...

The Issue: Stryker has received complaints associated with cracks and/or fracture of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Rim Impactor Tip Product Usage: Used for MDM Recalled...

The Issue: Stryker has received complaints associated with cracks and/or fracture of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Recalled by...

The Issue: A potential non conformance was identified with the Zero-P VA plate where...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Draeger Medical, Inc.

Recalled Item: Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended Recalled by...

The Issue: Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Ethicon Endo-Surgery Inc

Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...

The Issue: During aging studies, the firm determined that the gastric belts were unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Ethicon Endo-Surgery Inc

Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...

The Issue: During aging studies, the firm determined that the gastric belts were unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Ethicon Endo-Surgery Inc

Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...

The Issue: During aging studies, the firm determined that the gastric belts were unable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified customers regarding over stimulation or stimulation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Medtronic Neuromodulation

Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified customers regarding over stimulation or stimulation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2013· Bard Peripheral Vascular Inc

Recalled Item: Bard LifeStent Solo Vascular Stent Recalled by Bard Peripheral Vascular Inc...

The Issue: Bard Peripheral Vascular is recalling specific lots of Bard Lifestent Solo...

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

Class I — Serious Health HazardOngoing
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Prolifta Dietary Supplement Prolifta Recalled by Haute Health, LLC Due to...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: PHUK Sexual Enhancement Ultimate Pleasure Recalled by Haute Health, LLC Due...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Virilis Pro Recalled by Haute Health, LLC Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2013· Big Blue Fisheries

Recalled Item: Hickory Smoked King Salmon is sold in vacuum packed plastic packages...

The Issue: Big Blue Fisheries, LLC. is recalling ALL smoked products from all lots and...

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

Class II — Potential Health HazardOngoing
Refund