Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,332 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,332 in last 12 months

Showing 2412124140 of 27,157 recalls

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 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· 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 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 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 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 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 11, 2013· Zimmer, Inc.

Recalled Item: ZIMTRON 6 DEG 22 HEADS 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: 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· 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
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: FREE-LOCK LAG SCREW 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· GE Healthcare, LLC

Recalled Item: HGE Healthcare Patient Monitor B30 Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing