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. 2,520 recalls have been distributed to Maine in the last 12 months.
Showing 9481–9500 of 27,655 recalls
Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...
The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...
The Issue: Elevated rates of false negative results may occur when using blood culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098 Recalled by...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004 Recalled by...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit Catalog Number 70-6762 Recalled by Magellan...
The Issue: Magellan has received reports that control tests of either the Low-Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer...
The Issue: Fifty (50) individual units from Lot D20111130 were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2...
The Issue: Mislabeled product labeling incorrect length or height, or length and height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadia AN Interbody Convex 10x22x15mm Catalog Number: 6101-2102215NC-G2...
The Issue: Mislabeled product labeling incorrect length or height, or length and height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2...
The Issue: Mislabeled product labeling incorrect length or height, or length and height...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriIFit TS SIZE 2 Recalled by Corin Ltd Due to Units from one batch of...
The Issue: Units from one batch of TriFit TS size 2 stem were found to be labeled as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriFit CF SIZE 7 Recalled by Corin Ltd Due to Units from one batch of...
The Issue: Units from one batch of TriFit TS size 2 stem were found to be labeled as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear....
The Issue: Potential that a limited number of individual contact lens packages have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnera 400A Digital Radiographic System Recalled by Arcoma AB Due to There...
The Issue: There is the potential for the X-Ray system to short circuit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnera 400T Digital Radiographic System Recalled by Arcoma AB Due to There...
The Issue: There is the potential for the X-Ray system to short circuit due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System...
The Issue: Due to a software error, the user may lose functionality of the system or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WorkMate Claris v.1.2 Upgrade Kits Recalled by Abbott Laboratories Inc. (St...
The Issue: Due to a software error, the user may lose functionality of the system or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System...
The Issue: Due to a software error, the user may lose functionality of the system or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676) Siemens...
The Issue: Photometer Lamp May Reach Saturation Without Flagging Results, may generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CoV2 Ag calibrator (Product Code 6199950) - Product Usage: Recalled...
The Issue: Ortho investigated and confirmed the potential for unexpected failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...
The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.