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. 1,830 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,830 in last 12 months

Showing 2106121080 of 48,326 recalls

Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x30 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x100 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 2.5x170mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x36 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x32 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x105 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire HBS Sterile Lot Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Sterile Single Trochar Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x115 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x85 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x90 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 1.1x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT Model # 728332 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to In certain...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Model # 728321 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Vereos PET/CT Model # 882446 Recalled by Philips Medical Systems (Cleveland)...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to In...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT Model # 882456 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Model # 728231 Recalled by Philips Medical Systems (Cleveland)...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model # 728323 Recalled by Philips Medical Systems...

The Issue: In certain instances when performing a cardiac step and shoot acquisition...

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

Class II — Potential Health HazardOngoing