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. 1,034 recalls have been distributed to Minnesota in the last 12 months.
Showing 27061–27080 of 52,120 recalls
Recalled Item: Minivelle (estradiol transdermal system) 0.0375 mg/day Recalled by Noven...
The Issue: Defective Delivery System: no longer meets the specification for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Ingress of fluids into the device can affect various electronic circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Clip Gun Magazines are packaged in individually sealed pouches...
The Issue: The packaging sterile barrier does not comply with the applicable packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TVS LPA Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Drainer Centesis Catheter Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centeze Centesis Catheter Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducers Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elite HV Introducer Recalled by Galt Medical Corporation Due to The products...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) TVS LPA Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) ELITE HV Recalled by Galt Medical Corporation Due to The products listed...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Vascular Dilator Recalled by Galt Medical Corporation Due to The products...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...
The Issue: The diameter of the drill sleeve guide raw material was found to be under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...
The Issue: The bottles are mislabeled with an incorrect part number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...
The Issue: Possible transient electrical connection interruption between an HVAD System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...
The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.