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 4106141080 of 46,762 recalls

Medical DeviceNovember 5, 2013· Boston Scientific Corporation

Recalled Item: Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No...

The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...

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

Class II — Potential Health HazardOngoing
DrugNovember 4, 2013· Greenstone Llc

Recalled Item: Glipizide XL (glipizide) extended release tablets Recalled by Greenstone Llc...

The Issue: Failed Dissolution Specification; the bulk lot yielded an out of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2013· Pfizer Inc.

Recalled Item: Glucotrol XL (glipizide) extended release tablets Recalled by Pfizer Inc....

The Issue: Failed Dissolution Specification; 8 hr stability timepoint

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2013· Alexion Pharmaceuticals, Inc.

Recalled Item: Soliris (eculizumab) Concentrated Solution for Intravenous Infusion Only...

The Issue: Presence of Particulate Matter: Failed the appearance test for the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2013· IQ Formulations, LLC

Recalled Item: Hydravax High Potency Diuretic Weight Loss Solution Recalled by IQ...

The Issue: Marketed Without an Approved NDA/ANDA; this product is being recalled for...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 4, 2013· Medline Industries Inc

Recalled Item: Mucus Specimen Trap 40 cc Recalled by Medline Industries Inc Due to There is...

The Issue: There is a potential that the specified mucus specimen traps are not...

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

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

Recalled Item: Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin)...

The Issue: The patient label associated with the product may be incorrect in that the...

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 30MM 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 SUPER COMPLIANT 7MM X 15MM 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 150CM 2 TIP 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 GDC-18 360 18MM X 30CM Recalled by Stryker Neurovascular Due...

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 20MM 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 COMPLIANT 5MM X 30MM 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 COMPLIANT 4MM X 10MM 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 GDC-10 ULTRA SOFT 2MM X 3CM 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 J 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 EXCELSIOR SL-10 PRE-SHAPED J 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 EXCELSIOR SL-10 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 COMPLIANT 5MM 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 GDC VORTX 2MM X 3MM 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