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. 2,708 recalls have been distributed to Wisconsin in the last 12 months.
Showing 5981–6000 of 28,744 recalls
Recalled Item: DOLOMITE GLOSS ROLLATOR - intended to support during walking and Recalled by...
The Issue: Premature failure of the seat during use, the plastic eyelets of the folding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE Suction Coagulators Recalled by Megadyne Medical Products, Inc. Due...
The Issue: An issue with the Suction Coagulator product family may lead to fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: A medical device correction is being issued for SIGMA Spectrum Infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare Corporation Due...
The Issue: A medical device correction is being issued for SIGMA Spectrum Infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella LD intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.0 intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist intravascular micro axial blood pump Recalled...
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP with SmartAssist intravascular micro axial blood pump Recalled by...
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Direct Amplification Disc Kit Recalled by DiaSorin Molecular LLC...
The Issue: There is a potential for the direct amplification disc to malfunction which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 2.5 intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) Recalled by...
The Issue: Carryover from the Direct LDL-cholesterol assay on the Rx instruments may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2 Recalled...
The Issue: Dura regeneration matrix may have out-of-specification endotoxin levels due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. X-ray Image guided Therapy System. Recalled by PHILIPS...
The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.