Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,019 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,019 in last 12 months

Showing 78417860 of 52,570 recalls

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· Advance-Esthetic LLC

Recalled Item: MED-810A Zemits NDPrime Laser products Recalled by Advance-Esthetic LLC Due...

The Issue: Advance-Esthetic LLC failed to comply with the applicable standards...

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· Philips North America

Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to When preparing...

The Issue: When preparing for CCT Fluoroscopy mode and activating the CCT foot pedal...

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
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· Philips North America Llc

Recalled Item: Big Bore RT with software version V4.8.0.10421- Model: 728242 CT Recalled by...

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
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 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· 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