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. 2,439 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,439 in last 12 months

Showing 3864138660 of 52,120 recalls

FoodJuly 30, 2015· Whole Foods Market

Recalled Item: Whole Foods Market Recalled by Whole Foods Market Due to Undeclared Allergen

The Issue: Whole Foods Market is recalling CC & FP HSH Coconut Curry Cauliflower Salad...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 30, 2015· Nutrition Resource Services, Inc.

Recalled Item: JBN (Just Be Natural) Earth Superior Whey Banana Cream Pie Recalled by...

The Issue: Protein powders and nutritional supplement products made of whey...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2015· Wockhardt Usa Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...

The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2015· Wockhardt Usa Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...

The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2015· Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Recalled Item: Lisinopril Tablets Recalled by Vintage Pharmaceuticals LLC dba Qualitest...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Trauma Ex-Fix System (Small Recalled by Synthes (USA) Products LLC...

The Issue: Labeling changes were made related to MR conditions that align with standard...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: VEPTR Vertical Expandable Prosthetic Titanium Rib Recalled by Synthes (USA)...

The Issue: The last hole on certain VEPTR Inferior Cradles may be partially formed....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Multi-Access Port Closed Suction System for Adults Recalled by...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long Recalled by...

The Issue: Potential for micropores to form, allowing fluid to enter the hollow handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing