Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,749 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,749 in last 12 months

Showing 4564145660 of 52,120 recalls

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
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
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· 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 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· 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 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 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 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 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 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
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 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· 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 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 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 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 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 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