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. 1,655 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,655 in last 12 months

Showing 4090140920 of 46,762 recalls

Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Porous Patella Drill Guide-29mm dia./10mm...

The Issue: This is an expansion of the June 2013 recall of NexGen Micro components....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with 110cm tubing & 6mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 60cm tubing & 13mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 110cm tubing & 17mm cannula Recalled by...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Ultradent Products, Inc.

Recalled Item: Opal Orthodontics by Ultradent. Avex CX2 Ceramic Orthodontic Brackets Avex...

The Issue: Ultradent Products Inc. is recalling various lots of Avex CX2 Orthodontic...

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

Class III — Low RiskOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with 60cm tubing & 9mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2013· Vitality Research Labs LLC

Recalled Item: vitaliKOR Ready When You Are Recalled by Vitality Research Labs LLC Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Tendex

Recalled Item: P-BOOST Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Tendex

Recalled Item: NATURECT Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 19, 2013· Nexgen Pharma, Inc.

Recalled Item: PCC Recalled by Nexgen Pharma, Inc. Due to Nexgen Pharma Inc. is recalling...

The Issue: Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 1-1.5 HP Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Lite Blood Glucose Test Strips Recalled by Abbott Diabetes Care,...

The Issue: Certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 2-3 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 2-3 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing