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. 2,603 recalls have been distributed to Wisconsin in the last 12 months.
Showing 17621–17640 of 28,744 recalls
Recalled Item: LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600...
The Issue: Teleflex Medical is recalling the affected product because there may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol TC Reusable Electrodes (TCN) Recalled by Cosman Medical, LLC Due to...
The Issue: After multiple reprocessing cycles, the epoxy resin which holds the TCN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Recalled by Zimmer Biomet, Inc. Due to Finishing...
The Issue: Finishing guide does not adequately account for shape differences present in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heron toilet and bath chair Model 880505-01 & 880505-11 Recalled by R82 A/S...
The Issue: Replacement campaign on all units that have a gas spring head in aluminum.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye Recalled by Alcon Research, Ltd. Due to Some ORA...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Medical Charged-Particle Radiation Therapy System Recalled by Elekta,...
The Issue: The table shift in the vertical direction was inverted during the use of CMA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...
The Issue: Plastic heat exchanger fibers separating the blood compartment from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...
The Issue: Some ORA Carts have the potential to return an incorrect IOL power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Suction 9734308 Small AxiEM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Curved Suction 90 9733451 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Set Supplemental INS AxiEM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Instrument Kit 9733908 Fusion ENT Recalled by Medtronic...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Curved Suction 70 9733450 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Straight Suction 9733449 EM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.