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. 2,629 recalls have been distributed to Wisconsin in the last 12 months.
Showing 14401–14420 of 28,744 recalls
Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...
The Issue: There is no warning in the Elekta Unity manual for the administration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G-6-PDH Normal Control (G-6-PDH CONTROL N) Recalled by Randox Laboratories...
The Issue: The target values and ranges in these lots are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G-6-PDH Deficient Control (G-6-PDH CONTROL D) Recalled by Randox...
The Issue: The target values and ranges in these lots are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...
The Issue: There is a potential for the single use suction valve to come apart and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Incorrect part description contained on an additional label placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...
The Issue: Pin hole package failures compromising sterility of product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Video Laryngoscope Recalled by Verathon, Inc. Due to A...
The Issue: A typographical error in the Operations & Maintenance Manual incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...
The Issue: Stability did not meet acceptance criteria for visual appearance during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief Recalled by...
The Issue: Outflow Graft leaking at the pump connection during the implantation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to...
The Issue: Outflow Graft leaking at the pump connection during the implantation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ally Bone Screw - Product Usage:Bone Screws are indicated for Recalled by...
The Issue: There may be dimensional manufacturing error that represents a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestilix 1600X Prestilix system is a fully integrated remote controlled...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to There has been a reported...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silhouette VR This fully integrated system offers intuitive controls with...
The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.