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 7821–7840 of 28,744 recalls
Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...
The Issue: Potential communication issue in which the Vanta Clinician Programmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta Clinician Programmer Application Recalled by Medtronic Neuromodulation...
The Issue: Potential for Vanta Clinician Programmer Application (CP App) A71200...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare N1 TiUltra TCC NP 3.5x13mm Recalled by Nobel Biocare Due to...
The Issue: Due to the presence of a burr which may cause an aspiration risk to patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5" Recalled by Stradis...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NARMD MEDICAL DEPOT Scissors Iris Curved 4.5" Recalled by Stradis Medical,...
The Issue: The sterile barrier may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...
The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: There is a potential of the packaging not maintaining a sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin METAFIX HIP STEM Recalled by Corin Ltd Due to One MetaFix size 7...
The Issue: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...
The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...
The Issue: Due to a non-sterile component (tape) being place within the sterile portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.