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. 2,489 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,489 in last 12 months

Showing 2416124180 of 52,120 recalls

FoodJanuary 11, 2019· McCormick & Company, Inc. - Flavor Manufacturing Center

Recalled Item: El Guapo Pasilla-Ancho Chile Pods 2oz Recalled by McCormick & Company, Inc....

The Issue: Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 11, 2019· McCormick & Company, Inc. - Flavor Manufacturing Center

Recalled Item: El Guapo Chile Habanero Habanero Chili Pepper 0.5oz Recalled by McCormick &...

The Issue: Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 11, 2019· Lin-Zhi International Inc

Recalled Item: Ethyl Alcohol Enzymatic Assay Recalled by Lin-Zhi International Inc Due to...

The Issue: Shelf life of the product may be reduced due to degradation of the assay.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 11, 2019· AAP Implantate Ag

Recalled Item: aap Implante AG Recalled by AAP Implantate Ag Due to There is the potential...

The Issue: There is the potential for the Lambotte chisel to break at the welded piece...

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

Class II — Potential Health HazardOngoing
DrugJanuary 10, 2019· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid) Recalled by...

The Issue: Presence of Particulate Matter: filmy/cloudy particulate observed in vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2019· MAJOR PHARMACEUTICALS

Recalled Item: Losartan Potassium Tablets Recalled by MAJOR PHARMACEUTICALS Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2019· Bio-Rad Laboratories, Inc

Recalled Item: EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management...

The Issue: User-induced circumstances can contribute to the EVOLIS Microplate Processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: DELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14 PushValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Karl Storz Endoscopy

Recalled Item: Insufflation tubing to be used with varies insufflator units. Recalled by...

The Issue: The sterile single-use tubing may contain higher ethylene oxide (EO)...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Feeding Tube Metric Recalled by ConvaTec, Inc Due to An internal assessment...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Forceps Blue Recalled by ConvaTec, Inc Due to An internal assessment of...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC50 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing