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. 2,529 recalls have been distributed to Maine in the last 12 months.
Showing 6701–6720 of 27,655 recalls
Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...
The Issue: There is a potential that the distal end of the catheter may be bent beyond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edward Lifesciences Recalled by Edwards Lifesciences, LLC Due to There is a...
The Issue: There is a potential that the distal end of the catheter may be bent beyond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on...
The Issue: A component of a sub-assembly used in the affected AEDs had not undergone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clariti 1-day toric soft contact lenses Recalled by CooperVision, Inc. Due...
The Issue: The lenses manufactured in the affected lot were made with a misaligned axis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Anesthesia ES System (PAS ES) Recalled by CareFusion 303, Inc. Due...
The Issue: Automated dispensing cabinet drawer firmware may have inadvertently been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brainlab ExacTrac Dynamic software Recalled by Brainlab AG Due to Deep...
The Issue: Deep Inspiration Breath Hold (DIBH) functionality may not work as specified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus Exchange Kit Therapeutics. Component of Amicus Separator...
The Issue: Potential for centrifuge packs to develop a stress leak for certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amicus MNC Apheresis Kit Double Needle. Component of Amicus Separator...
The Issue: Potential for centrifuge packs to develop a stress leak for certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Global Total LP single step medium Recalled by CooperSurgical, Inc. Due to...
The Issue: It has come to CooperSurgical's attention that the affected Product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre Reader Recalled by Abbott Diabetes Care, Inc. Due to...
The Issue: Lithium-ion batteries in glucose monitoring system readers may swell,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to Firm has...
The Issue: Firm has initiated a removal of the product due to insufficient evidence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DreamStation Auto BiPAP and CPAP Recalled by Philips Respironics,...
The Issue: A limited number of remediated Philips DreamStation units may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II ROODRA non-invasive vascular diagnostic device Recalled...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II REVO non-invasive vascular diagnostic device Recalled by...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device...
The Issue: The current luer fittings and adaptors allow for the possibility of the air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 App Recalled by Abbott Diabetes Care, Inc. Due to If using...
The Issue: If using affected glucose monitoring app on Android 13 Operating System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal SafeLiner Suction Canister Recalled by DeRoyal Industries Inc Due to...
The Issue: The reason for the voluntary recall is due to shrinkage of the canister lid....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.