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. 2,662 recalls have been distributed to Wisconsin in the last 12 months.
Showing 12221–12240 of 28,744 recalls
Recalled Item: Phillips Azurion 7 M20 Recalled by Philips North America, LLC Due to No...
The Issue: No torque was specified for the four screws that connect the gearbox and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices s intended to be used Recalled...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended...
The Issue: The Coupler size labeling of the outer tray may not match the Couper size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips V60 Ventilators with Power Management PCBA part number 1055906...
The Issue: Solder connection failure on Power Management printed circuit board assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: natus newborn care Olympic Brainz Monitor Recalled by Natus Neurology DBA...
The Issue: The OBM system functional test (impedance and noise) was not carried out on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA - Deficient VIII Recalled by Diagnostica Stago, Inc. Due to A risk of...
The Issue: A risk of sample-to-sample cross-contamination of Emicizumab for factor VIII...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation standalone software treatment planning system Recalled by...
The Issue: Due to physical limitations of the treatment machine, the maximum field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000F with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product...
The Issue: Bolts holding the longitudinal movement of catheterization tables may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake System Recalled by Capintec Inc Due to It is...
The Issue: It is possible that the collimators have screw hole locations that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merits E604 Pilot Navigator Stairlift - Product Usage: To transport Recalled...
The Issue: Pinion gear may disengage from track allowing lift to slip or jolt.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReWalk Personal 6.0 Recalled by Argo Medical Technologies Ltd Due to ReWalk...
The Issue: ReWalk Robotics received two complaints (one in the US; one in the Germany),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product...
The Issue: Cases of Portex¿ Lumbar Puncture Tray Child, SKU #4826PL-20 had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 Software Upgrade Kit Recalled by Abbott Due to Internal...
The Issue: Internal testing of software identified software anomaly scenarios where if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: uDR 596i Digital Medical X-Ray Imaging System - Product Usage: Recalled by...
The Issue: Two issues were identified with the stationary x-ray system. 1. Some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Editing an assay Test Definition and switching to another assay s Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x4 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4oz. Tube Recalled by Gentell, Inc Due to During an FDA...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.