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. 2,404 recalls have been distributed to Maine in the last 12 months.
Showing 18601–18620 of 27,655 recalls
Recalled Item: Access Ostase Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Ostase QC Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMsealer Open Shears. Model FM3001 Recalled by Domain Surgical, Inc. Due to...
The Issue: Domain Surgical, Inc. announces a voluntary field action for the FMsealer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...
The Issue: Recovery of Incorrect Isocenter -operational change
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...
The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens is providing software update version VA50A_SP3 to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...
The Issue: Software defect:2D projection of contours in Verity. The defect causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...
The Issue: A product issues happens for RF projection images. If user measures on RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes....
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...
The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Sterile Disposable Probes sold individually Recalled by Ultroid...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash system Recalled by Siemens Medical Solutions USA,...
The Issue: Hardware issue that may expose the user to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS system Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Hardware issue that may expose the User to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (50 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.