Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,666 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,666 in last 12 months

Showing 54615480 of 29,186 recalls

Medical DeviceOctober 10, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP Emergency Drive Recalled by Maquet Medical Systems USA Due to...

The Issue: Product removal due to possible blocking or impairment of the CARDIOHELP...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 9, 2023· Philips North America

Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to This recall is...

The Issue: This recall is part of a 2-issue recall for the same system. When using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Biomet, Inc.

Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...

The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...

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

Class II — Potential Health HazardOngoing