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 5881–5900 of 27,655 recalls
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. X-ray Image guided Therapy System. Recalled by PHILIPS...
The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 and FD20. X-ray Imaging System. Recalled by PHILIPS MEDICAL...
The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxylog 3000 Plus emergency and transport ventilator Recalled by Draeger...
The Issue: Draeger has become aware of instances where the device stopped working when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Amplatzer Steerable Delivery Sheath (ASDS) Recalled by Abbott Due to...
The Issue: There is an overall reported incidence rate of 0.77% related to observed or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi/X Tip-Up Fenestrated Grasper Recalled by Intuitive Surgical,...
The Issue: Fenestrated Graspers have a manufacturing issue has the potential to cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Short Recalled by Tornier, Inc Due...
The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEQUALIS FLEX REVIVE Assembly Screw 0mm Recalled by Tornier, Inc Due to A...
The Issue: A comingle/swap resulted in the labeling and laser marking on the product to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Resection Electrodes - HF resection electrodes are part of Recalled by...
The Issue: Additional Caution statements in IFU: (1) Due to complaints where the loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Recalled by Argon Medical Devices, Inc Due to There is...
The Issue: There is the potential that the vena Cava Filter may not perform as intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus BRONCHOFIBERSCOPE BF Type Recalled by Olympus Corporation of the...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus BRONCHOVIDEOSCOPE Recalled by Olympus Corporation of the Americas...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus Corporation...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OES BRONCHOFIBERSCOPE BF Type Recalled by Olympus Corporation of the...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus BRONCHOVIDEOSCOPE BF Type Recalled by Olympus Corporation of the...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA II BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeamAdjust software Version 2.3.3 The following devices are Recalled by...
The Issue: Generated calibration file will not be correct in case of a relative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRED Flow Re-Direction Endoluminal Device Recalled by MICROVENTION INC. Due...
The Issue: Intracranial aneurysm flow diverter device may be manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.