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.

52,482 total recalls
2,515 in last 12 months

Showing 2556125580 of 28,744 recalls

Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...

The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Healthcare Informatics, Inc.

Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...

The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...

The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 12/14 UNIPOLAR FEMORAL HE VERSYS CEM LD/FX SZ 11X12 VERSYS Recalled by...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: MODULAR AUSTIN MOORE FENE. Item codes starting with 45502001 Recalled by...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR Recalled by...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: FEM HD ION (various sizes) Recalled by Zimmer, Inc. Due to Zimmer recently...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: HERBERT MINI BONE SCREW 2 and HERBERT/WHIPPLE C ANN BONE. Recalled by...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System: One 1 g...

The Issue: Incorrect instructions for use (IFU).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: ITST ANTI-ROTATION SCREW and FEM IM NAIL (10MM Recalled by Zimmer, Inc. Due...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: VERSYS HERITAGE FEM STEM Recalled by Zimmer, Inc. Due to Zimmer recently...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing