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. 2,467 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,467 in last 12 months

Showing 3306133080 of 52,120 recalls

FoodNovember 15, 2016· 4 C Foods, Corp.

Recalled Item: Cento Romano Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...

The Issue: FDA sample revealed the presence of Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Smith & Nephew, Inc.

Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...

The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...

The Issue: Software update that provides software and firmware bug-fixes to improve...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2016· Encore Medical, Lp

Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...

The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...

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

Class II — Potential Health HazardOngoing
DrugNovember 14, 2016· Akorn Inc

Recalled Item: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...

The Issue: Failed Stability Specifications; out-of specification value for homogeneity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 14, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips Spectral CT Applications supports viewing and analysis of images...

The Issue: A software defect is causing issues with the IQon Spectral CT and Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT is a Computed Tomography X-Ray System intended Recalled by...

The Issue: A software defect is causing issues with the IQon Spectral CT and Philips...

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

Class II — Potential Health HazardOngoing
DrugNovember 13, 2016· Ultimate Body Tox

Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 12, 2016· KRAFT HEINZ FOODS COMPANY

Recalled Item: Weight Watchers Smart Ones Recalled by KRAFT HEINZ FOODS COMPANY Due to...

The Issue: Possible contamination of product with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2016· Cedar Crest Specialties, Inc.

Recalled Item: Cedar Crest Monster Cookie Dough Ice Cream in 3 Gallon container. Recalled...

The Issue: The cookie dough used in select ice creams may be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2016· Cedar Crest Specialties, Inc.

Recalled Item: Cedar Crest Chocolate Chip Cookie Dough Ice Cream packaged in Recalled by...

The Issue: The cookie dough used in select ice creams may be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2016· Cedar Crest Specialties, Inc.

Recalled Item: Cedar Crest Pirate's Bounty Ice Cream 1.5 quarts (1419 mL) Recalled by Cedar...

The Issue: The cookie dough used in select ice creams may be contaminated with Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...

The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...

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

Class II — Potential Health HazardOngoing
FoodNovember 10, 2016· American Blue Ribbon Holdings DBA Legendary Baking

Recalled Item: Ultimate Chocolate Chip Cookie Dough Pie Recalled by American Blue Ribbon...

The Issue: Product incorporated cookie dough that was potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund