Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,536 recalls have been distributed to Maine in the last 12 months.
Showing 5341–5360 of 27,655 recalls
Recalled Item: VITROS 4600 Chemistry System Product Code 6802445 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Product Code 6844461 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Product Code 6802413 and Product Recalled by...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Product Code 6802783 and Product...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.