Product Recalls in Wisconsin
Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,624 recalls have been distributed to Wisconsin in the last 12 months.
Showing 15981–16000 of 28,744 recalls
Recalled Item: Foley Temperature Sensor Catheter 8FR Recalled by Degania Silicone, Ltd. Due...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 14FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 14FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 18FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 10FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 12FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL GC-Lect Agar Recalled by Becton Dickinson & Co. Due to A portion of...
The Issue: A portion of this lot was manufactured using Gentamicin instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.