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. 2,478 recalls have been distributed to Minnesota in the last 12 months.
Showing 27081–27100 of 52,120 recalls
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: 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) 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: 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.
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: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loxapine Capsules Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: GMP Deviations: a recent FDA inspection of the manufacturing site revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection Recalled by AuroMedics Pharma LLC...
The Issue: Presence of Particulate Matter: confirmed customer report for presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ampicillin and Sulbactam for Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Presence of Particulate Matter: confirmed customer report of the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zeego Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Interventional Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: If the C-arm is manually moved in the longitudinal direction to a fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.