Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,071 recalls have been distributed to Montana in the last 12 months.
Showing 5901–5920 of 27,852 recalls
Recalled Item: Ingenia Elition X 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: 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: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
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: 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: 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: 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: 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: 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 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 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 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: 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 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: 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.
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 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.