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. 1,102 recalls have been distributed to Wisconsin in the last 12 months.
Showing 12141–12160 of 28,744 recalls
Recalled Item: Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/...
The Issue: The hemostasis valve of aspiration guide catheter devices may fail to seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Utak NR Trace Elements Serum Control Recalled by Utak Laboratories Inc Due...
The Issue: The product has an incorrect value for cadmium and an incorrect expected range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifePAK 500 Automated External Defibrillator Recalled by Physio-Control,...
The Issue: Automated External Defibrillators may not detect a patient connection due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replaceable lead set for the Wireless Acquisition Module (WAM) Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4 and patient cable for the S4 Wireless Telemeter with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H12+ and patient cable for the H12+ Holter Recorders with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X12+ and patient cable for the X12+ Telemeter with the Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor Recalled...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lead diagnostic electrocardiograph under the following device names: ELI 10...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
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: 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: 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: 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: 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: 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.