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. 2,621 recalls have been distributed to Minnesota in the last 12 months.
Showing 13221–13240 of 29,186 recalls
Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for...
The Issue: Power supply (Model Number: TLC-2003) ME90A2403F01 (24 VDC, 3.75 A, 90 W, 1%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Potential for calibration error resulting in QC failures after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...
The Issue: The firm has become aware there is a potential problem with its DABRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/wing 5700LAX...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...
The Issue: Fetal transducers distributed in advance of receiving 510(k) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...
The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.