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. 1,129 recalls have been distributed to Wisconsin in the last 12 months.
Showing 6801–6820 of 28,744 recalls
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...
The Issue: Battery leakage can cause corrosion to the metal enclosure near the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...
The Issue: Distributed sample collection kit with an unapproved instruction for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...
The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flex-Neck Catheter External Repair Kit LOT CE-1400/A Recalled by Merit...
The Issue: Product that was built for design verification testing was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM Recalled by...
The Issue: The subject product lots are being recalled because they received a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.