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. 2,662 recalls have been distributed to Wisconsin in the last 12 months.
Showing 12241–12260 of 28,744 recalls
Recalled Item: NAVIO Soft Tissue Protector Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential for the NAVIO Soft Tissue Protector to become stuck or bound to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x8 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CapsoCam Plus (SV-3) Recalled by Capso Vision, Inc. Due to Ingestible...
The Issue: Ingestible video capsule system has capsule with incorrect capture mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A...
The Issue: Philips has received a number of reports of HeartStart MRx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexus Universal with OptiBond Universal Recalled by Kerr/Pentron, DBA Kerr...
The Issue: An issue within production process used to package trial kits let to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...
The Issue: The firm is providing validated cleaning and disinfection instructions in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test Recalled by Qiagen Sciences LLC Due to An image on the...
The Issue: An image on the associated polybag contains an incorrect rinse time of 30...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...
The Issue: Reports have been received about the transcutaneous monitoring system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software...
The Issue: Menu selections for users to access the oxygen (O2) sensor calibration were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...
The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...
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.