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. 2,557 recalls have been distributed to Wisconsin in the last 12 months.
Showing 20041–20060 of 28,744 recalls
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...
The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mentor MemoryGel Breast Implant Recalled by Mentor Texas, LP. Due to The box...
The Issue: The box of 300cc MemoryGel Breast Implant was labeled with null...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...
The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...
The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...
The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...
The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...
The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...
The Issue: TRYX products are being recalled since the processes of spaying, welding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Tray Recalled by C.R. Bard, Inc. Due to Labeling problem
The Issue: Labeling problem
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...
The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.