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. 1,098 recalls have been distributed to Wisconsin in the last 12 months.
Showing 12261–12280 of 28,744 recalls
Recalled Item: Custom procedure trays containing medical components needed to facilitate...
The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedure trays containing medical components needed to facilitate...
The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedure trays containing medical components needed to facilitate...
The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedure trays containing medical components needed to facilitate...
The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedure trays containing medical components needed to facilitate...
The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedure trays containing medical components needed to facilitate...
The Issue: The medical procedure trays contain one or more recalled surgical gowns. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Tests returning incorrect...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...
The Issue: hearing performance degradation due to body-fluid entering the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Ethyl Alcohol Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The assay may exhibit a positive bias in QC and patient results within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Pipeline Flex Embolization Device. For neurological endovascular use....
The Issue: Embolization device delivery system may fracture at the distal section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS....
The Issue: Embolization device delivery system may fracture at the distal section...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Cogent Hemodynamic Monitoring System. Recalled by ICU Medical, Inc. Due...
The Issue: Firm identified software issues which leads to the patient ID and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee Biplane Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A software issue could potentially cause the stand and table movements to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.