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 20101–20120 of 28,744 recalls
Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# e4001-00 The Anastoclip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...
The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is...
The Issue: Devices were incorrectly programmed during manufacturing therefore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babytherm 8004/8010 Recalled by Draeger Medical, Inc. Due to Risk associated...
The Issue: Risk associated with operating the device in skin temperature mode with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynasty Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...
The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...
The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba Mindray...
The Issue: Potential for a leak to occur on the back-up O2 and air e-size cylinder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.