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. 1,043 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,043 in last 12 months

Showing 14021–14040 of 27,852 recalls

Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Recalled by...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing