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. 2,622 recalls have been distributed to Minnesota in the last 12 months.
Showing 12241–12260 of 29,186 recalls
Recalled Item: Clip Applier Kit Recalled by Applied Medical Resources Corp Due to There may...
The Issue: There may be a slightly protruding rivet on the distal end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...
The Issue: There may be a slightly protruding rivet on the distal end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...
The Issue: There may be a slightly protruding rivet on the distal end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge Recalled by...
The Issue: Iincorrectly packaged without the required lidocaine as labeled
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew FOOTPRINT Ultra PK Suture Anchor Recalled by Smith & Nephew,...
The Issue: Space between the device and the packaging permits excessive movement which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Recalled by Rayner...
The Issue: RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...
The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 Part Number: 72202901...
The Issue: Space between the device and the packaging permits excessive movement which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jamshidi Bone Marrow Biopsy/Aspiration Needle Recalled by Bard Peripheral...
The Issue: Sterility compromised due to packaging pouches that may not be sealed properly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter 6F Model 5540. For delivery of Recalled by...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.