Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,771 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,771 in last 12 months

Showing 54415460 of 29,154 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 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
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· 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 Oncology with software version V4.8.0.10421...

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