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. 2,519 recalls have been distributed to Minnesota in the last 12 months.
Showing 19301–19320 of 29,186 recalls
Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...
The Issue: An incorrect sterility status on the label, non-sterile products labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...
The Issue: Potential performance issue on strain categorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Air 6 ENT Microscope Microscope examination of the human ear Recalled...
The Issue: The microscope may tip over if attachments are fully extended in one line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion Pump Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Depleted Battery alarm shows instead of Replace Battery. On battery power,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Radial Head Prosthesis System Recalled by Synthes (USA) Products LLC...
The Issue: There is the possibility that the radial stem may loosen post-operatively at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-115: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-110: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-112: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 900-130: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intact Disposable Wands (part of the Intact System) 777-120: 5 Recalled by...
The Issue: Product sterility compromised due to breach of sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo EZ Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell from...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFX Endovascular AAA System Recalled by Endologix Due to Endologix updated...
The Issue: Endologix updated the Instructions for Use (IFU) and implemented...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo DRF Recalled by Villa Sistemi Medicali S.P.A. Due to Patient fell...
The Issue: Patient fell from the table because the footrest of the device detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.