Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,729 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,729 in last 12 months

Showing 79017920 of 53,528 recalls

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
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· Philips North America Llc

Recalled Item: Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT...

The Issue: For oncology users: If the user performed off-set reconstruction on CT...

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

Class II — Potential Health HazardOngoing