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. 2,696 recalls have been distributed to Wisconsin in the last 12 months.
Showing 8301–8320 of 28,744 recalls
Recalled Item: Avanos Cortrak 2 Enteral Access System (EAS) Recalled by Avanos Medical,...
The Issue: Product labeling is being modified. STOP using the Anonymous Account Mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS Recalled by...
The Issue: Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIA Radiation Therapy Management (RTM) VERSIONS 13.6 Recalled by Varian...
The Issue: Software issue for treatment plan and image management application may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic Gastrovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: regard Clinical Packaging...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinici X da Vinci Xi Sureform 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: As a result of complaint data review, it identified tissue pushout events...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LetsGetChecked Blood Sample Collection kit-In vitro diagnostic medical...
The Issue: Users received sample collection kits that were assigned to another user....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Separation Technology Creamatocrit Plus Recalled by Stanbio Laboratory, LP...
The Issue: The device was being marketed as an IVD without a 510(k). Therefore,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology Recalled...
The Issue: Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.