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. 2,515 recalls have been distributed to Wisconsin in the last 12 months.
Showing 27021–27040 of 28,744 recalls
Recalled Item: Specialist 2 IM Rod Recalled by DePuy Orthopaedics, Inc. Due to Potential...
The Issue: Potential for the IM rod to break, leaving fragments in the patient....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineNet Anterior Cervical Cage Recalled by SpineNet Due to The recall...
The Issue: The recall decision has been made because because it has recently been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: Observed instability of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoGastric Solutions EsophyX2 Plus Device with Serosa Fastener and...
The Issue: EsophyX2Plus device was not validated under actual or simulated use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to Incorrect...
The Issue: Incorrect packaging of regular set and fast set cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gen-Probe LIFECODES PF4 Enhanced assay Recalled by Genetic Testing...
The Issue: Lifecodes PF4 Enhanced assay, lot number 3000389, is being recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to Frequent Proximal...
The Issue: Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Frequent Proximal...
The Issue: Frequent Proximal Occlusion Alarms (POAs) occurring on Symbiq devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to Symbiq Infusers...
The Issue: Symbiq Infusers have the potential to experience a white screen during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...
The Issue: A possible interruption of therapy when an E321 error code occurs while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.