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 5901–5920 of 27,655 recalls
Recalled Item: Vios Monitoring System Bedside Monitor Recalled by Murata Vios, Inc. Due to...
The Issue: A premature failure condition was identified with the L2050R pulse oximeter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Implant Kit Recalled by...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy...
The Issue: 1. Wheels loosening over time with use of the device could lead to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Reagent Pack Recalled by...
The Issue: Reagent packs could potentially contain incorrect wells, which will generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Calibrators Recalled by...
The Issue: Reagent packs could potentially contain incorrect wells, which will generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Select VA 21 with FD- A Mobile X-ray system Recalled by Siemens Medical...
The Issue: Incorrect glue was applied on the plexiglass sheet on the single tank cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options¿ / Epidural anesthesia kit (10 count carton) Recalled by B....
The Issue: Kits were assembled with the incorrect Filter Straw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Ergo Impactor Handle Recalled by Exactech, Inc. Due to The ball and...
The Issue: The ball and spring housed within the locking mechanism of the handle can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Clostridium difficile Nucleic Acid Test Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Enteric Pathogens Nucleic Acid Test (EP) Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.