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. 2,526 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,526 in last 12 months

Showing 93619380 of 27,852 recalls

Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Outflow Graft Recalled by Heartware, Inc. Due to Medtronic is...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Accessories Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Driveline Extension Cable Recalled by Heartware, Inc. Due to...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Implant Kit Recalled by Heartware, Inc. Due to Medtronic is...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Implant Kit Recalled by Heartware, Inc. Due to Medtronic is...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Axonics Modulation Technologies, Inc.

Recalled Item: BULKAMID Recalled by Axonics Modulation Technologies, Inc. Due to Lack of...

The Issue: Lack of Sterility Assurance; needle in procedure pack labeled as sterile may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Medtronic Neuromodulation

Recalled Item: Medtronic StimLoc Burr Hole Cover Recalled by Medtronic Neuromodulation Due...

The Issue: Excess nylon flash on the clip.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2021· Biomet, Inc.

Recalled Item: Arcos Modular Revision Hip System High Offset Cone Prox Body Recalled by...

The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...

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

Class II — Potential Health HazardOngoing