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. 2,589 recalls have been distributed to Minnesota in the last 12 months.
Showing 15121–15140 of 52,120 recalls
Recalled Item: BD Nexiva Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to...
The Issue: There is a breach in the product packaging that renders the product non-sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vit Kit-Freeze is intended for use in assisted reproductive procedures...
The Issue: Due to a component in kit being labeled with the incorrect Expiration Date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Helium Indicator on the Cardiosave display may over represent the amount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may unexpectedly shut down when the device is running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: De Wafelbakkers 18 ct Buttermilk Pancakes NET WT 1 lb. Recalled by De...
The Issue: Potential to contain Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nox T3s Recorder - Product Usage: intended for ambulatory recording Recalled...
The Issue: Error in the device firmware results in the inaccurate detection of device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra-Myossage Lotion 1-gallon bottle Recalled by DJO, LLC Due to Ultrasound...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEL CONDUCTOR Recalled by DJO, LLC Due to Ultrasound gels and lotions...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promethazine With Codeine Oral Solution Recalled by Morton Grove...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valproic Acid Oral Solution USP Recalled by Morton Grove Pharmaceuticals,...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Promethazine Syrup Plain Recalled by Morton Grove Pharmaceuticals, Inc. Due...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMINOSYN II 15% An Amino Acid Injection Recalled by ICU Medical Inc Due to...
The Issue: Presence of Particulate Matter: Particulate matter identified as fibers,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Injection Recalled by Meitheal Pharmaceuticals Inc Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: cobas EGFR Mutation Test v2-Somatic gene mutation detection system Catalog...
The Issue: False Mutation Detected results for the exon 20 insertion (Ex20Ins) mutation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flower E-Kit Recalled by Flower Orthopedics Corporation Due to Product kit...
The Issue: Product kit missing CDG 200 (Cannulated Countersink for 3.0-4.5mm Screws)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI Recalled by Welch Allyn Inc Mortara Due to The devices malfunction under...
The Issue: The devices malfunction under specific operator workflows.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030H Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.