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. 2,371 recalls have been distributed to Maine in the last 12 months.
Showing 22981–23000 of 27,655 recalls
Recalled Item: Cloward Spanner gauges are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cushing perforating drills are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVB distraction screws are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium fixation screws Recalled by Instrumed International, Inc. Due to...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galt trephines are bone cutting and drilling instruments that are Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xoran MiniCAT X-ray imaging device Recalled by Xoran Technologies, LLC Due...
The Issue: Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has become aware of a potential safety issue involving missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: The software issue described was corrected in the modification to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...
The Issue: Misbranding: Although the product labeling identifies the catheters as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Distal Reamer Extension Non Sterile Intended as Recalled by DePuy...
The Issue: Specific lots are being recalled due to the potential for the tabs to break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos Agile Max system The Luminos Agile is intended Recalled by...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Uroskop Omnia Max system The Uroskop Omnia is a Recalled by Siemens...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Max system The Ysio Max is a radiographic system used in...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.