Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,932 recalls have been distributed to Ohio in the last 12 months.
Showing 25001–25020 of 30,087 recalls
Recalled Item: D'errico perforator 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The Issue: The reason these devices are being withdrawn from the market by Instrumed is...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: 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: Schoitz weights are manual devices used with Schoitz tonometers and 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The Issue: The reason these devices are being withdrawn from the market by Instrumed is...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: A circumcision clamp is an instrument used to compress the Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...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: An endometrial suction curette is a device used to remove Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...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: McKenzie Perforator 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The Issue: The reason these devices are being withdrawn from the market by Instrumed is...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: Manual bunnell cranial drills are bone cutting and drilling instruments...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...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: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...
The Issue: The pediatric breathing circuits can crack prior to and during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
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: 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: 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: Vantage Panoramic X-Ray System used to perform dental and orthodontic...
The Issue: Failure of the primary collimator may result in unintentional movement of...
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: 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: 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: 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 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.