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. 1,759 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,759 in last 12 months

Showing 4268142700 of 52,120 recalls

Medical DeviceOctober 6, 2014· Zimmer Surgical Inc

Recalled Item: UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric...

The Issue: Non-injury complaints from Europe identified a malfunction that made it...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay Systems Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· PEROUSE MEDICAL

Recalled Item: Synthes Inflation System (03.804.4135) Product Usage: Inflation system is...

The Issue: Additional instructions for use due to inability to raise the pressure above...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Baxter Healthcare Corp.

Recalled Item: HomeChoice Automated PD system and HomeChoice Pro Automated PD system...

The Issue: There are additional and updated warning and cautions that are not in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i SYNCHRON Access Clinical Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
DrugOctober 3, 2014· Sagent Pharmaceuticals Inc

Recalled Item: Ketorolac Tromethamine INJECTION Recalled by Sagent Pharmaceuticals Inc Due...

The Issue: Incorrect or Missing Lot and/or Exp Date: Ketorolac Tromethamine Injection,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2014· Wisconsin Pharmacal Company

Recalled Item: CVS pharmacy Recalled by Wisconsin Pharmacal Company Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: CVS Pharmacy Pain Relieving...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 3, 2014· Monteris Medical Corp

Recalled Item: SideFire Directional Laser Probe Recalled by Monteris Medical Corp Due to...

The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Monteris Medical Corp

Recalled Item: FullFire Diffusing Tip Laser Probe Recalled by Monteris Medical Corp Due to...

The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
FoodOctober 2, 2014· Family Dollar Stores - NC Distribution Center

Recalled Item: Family Gourmet Long Grain Enriched White Rice in 32 oz. Recalled by Family...

The Issue: Possible insect infestation

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2014· Sandoz, Inc

Recalled Item: candesartan cilexetil Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An Out of Specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2014· Valeant Pharmaceuticals International

Recalled Item: Locoid (hydrocortisone butyrate 0.1%) Recalled by Valeant Pharmaceuticals...

The Issue: Subpotent Drug; for the active, HCB, and preservatives, Propylparaben and...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2014· Valeant Pharmaceuticals International

Recalled Item: Hydrocortisone Butyrate Cream 0.1% Recalled by Valeant Pharmaceuticals...

The Issue: Subpotent Drug; for the active, HCB, and preservatives, Propylparaben and...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 2, 2014· Zimmer, Inc.

Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...

The Issue: Failed to meet established requirements for sterile barrier integrity due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Medartis, Inc.

Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...

The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...

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

Class II — Potential Health HazardOngoing