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. 1,072 recalls have been distributed to Ohio in the last 12 months.
Showing 18101–18120 of 55,415 recalls
Recalled Item: MH-200S Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bransist Safire Recalled by Shimadzu Medical Systems Due to The firm has...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinias Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite Freelite Mx Kappa Free Kit .M.OPT.A Recalled by The Binding Site...
The Issue: Due to customer complaints of positive bias impacting quality control. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENNOVATE MIS REMOVALKEY SHORT Recalled by Aesculap Implant Systems LLC Due...
The Issue: Fracture or breakage of the spinal fixation arm at the downtube instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kaiser Permanente Clotrimazole Cream USP Recalled by Taro Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: H-E-B - Athlete's Foot Cream Clotrimazole Cream USP Recalled by Taro...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Best Choice Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Athlete's Foot Cream Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: An unknown degradation...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kollidon CL-M Crospovidone Ph.Eur.Type B Recalled by BASF Corporation Due to...
The Issue: Cross contamination: the excipient was found to be contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.