Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 909 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
909 in last 12 months

Showing 42801–42820 of 48,326 recalls

Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 2.7 X 6 CORT SCREW/SELFTA 2.7 X 7 CORT SCREW/SELFTA Recalled by Zimmer, Inc....

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: 1.5 X 6 CORT SCREW HEX/SE 2.0 X 6 CORT Recalled by Zimmer, Inc. Due to...

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: PRESSFIT FEM ST FX 16 X 1 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: 3.5 X 10 CORT SCREW SELFT 3.5 X 12 CORT Recalled by Zimmer, Inc. Due to...

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 36 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: 12/14 COCR FEMORAL HEAD (2 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: VERSA-FX KEYLESS 90D X 8 and X 11 Recalled by Zimmer, Inc. Due to Zimmer...

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: RECON SCREW LG 5.5MM DIA and M/DN FEM IM NAIL 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: CPT DEGREE TAPER (various sizes) and FEMORAL HD (various sizes) 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: 3.5 COMP PLT Recalled by Zimmer, Inc. Due to Zimmer recently conducted a...

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: DISTAL MEDIAL FEMORAL CON 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: 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: PERI SCR. 3.5MM X 10MM PERI SCR. 3.5MM X 12MM 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· 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
Medical DeviceOctober 11, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: If the couch, with the footrest extension attached, is positioned where the...

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

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

Recalled Item: ONE-PIECE LAG SCREW 11MM. Item codes starting with 00225900. 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