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 4108141100 of 46,762 recalls

Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED S 15OCM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand SUPER COMPLIANT 4MM X 7MM Recalled by Stryker Neurovascular...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED 90 150CM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 4MM X 15MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR 1018 PRE-SHAPED 45 150CM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED C 15OCM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Lanx, Inc.

Recalled Item: LANX Timberline MPF Lateral Modular Plate Fixation System Straight Split...

The Issue: Lanx, Inc. is recalling various lots of Timberline MPF Straight Split Tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Dekompressor Percutaneous Discectomy Probe. The Dekompressor is a single use...

The Issue: Stryker has identified a potential for the auger and/or cannula to fracture...

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

Class II — Potential Health HazardOngoing
DrugNovember 1, 2013· Greenstone Llc

Recalled Item: Nifedipine Recalled by Greenstone Llc Due to Labeling: Incorrect or Missing...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· Sigma-Tau Pharmaceuticals, Inc.

Recalled Item: PEGASPARGASE ONCASPAR Injection Recalled by Sigma-Tau Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility: Sigma-Tau PharmaSource, Inc. is conducting a...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Acetabular Pressurizer Recalled by Stryker Instruments Div. of Stryker...

The Issue: On March 14, 2013 a Work Order was opened for 120 units (20 boxes) of the...

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2013· Fresenius Kabi USA, LLC

Recalled Item: Tranexamic Acid Injection USP Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter: Particulate matter consistent with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions...

The Issue: Hospira has received customer reports of broken door assemblies on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral...

The Issue: Broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 31, 2013· Zimmer, Inc.

Recalled Item: NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen...

The Issue: Two complaints were received in which it was reported that the stem would...

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

Class II — Potential Health HazardOngoing
FoodOctober 30, 2013· National Enzyme Co

Recalled Item: Dietary Supplements packaged in the following configurations: (1) Carbo...

The Issue: Firm is recalling dietary supplements containing a raw material which may...

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

Class II — Potential Health HazardOngoing
Refund