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. 2,487 recalls have been distributed to Ohio in the last 12 months.
Showing 45101–45120 of 55,415 recalls
Recalled Item: Golden Corral MEATLOAF MIX #18028 Recalled by Processed Foods, Inc.- Custom...
The Issue: Products contain eggs which were recalled due to susceptibility to premature...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by...
The Issue: It was determined that a defective sieve bed subassembly enabled zeolite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...
The Issue: There is a potential for unintended and erratic motion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GMK Intramedullary Extension Rod 100 mm is a rod to Recalled by Medacta Usa...
The Issue: Medacta has registered in its database 3 cases of breakage of the GMK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mars Chocolate North America Milk Chocolate M & M's Net Recalled by Mars...
The Issue: Mars Chocolate North America is recalling M & Ms due to undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MaxLock Extreme Mod-Foot Concave Reamer Recalled by Orthohelix Surgical...
The Issue: Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...
The Issue: Customer complaints were received for positive bias reported on the controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has recently become aware of a potential safety issue to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z- GAS II EFFERVESCENT GRANULES Antacid/Antiflatulent Recalled by Bracco...
The Issue: Subpotent Drug: Out of Specification (OOS) result during routine stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Kit Recalled by Arrow...
The Issue: Arrow International, Inc. has initiated a voluntary recall for product code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 instrument for the da Vinci Si System Recalled by...
The Issue: Intuitive is issuing an urgent product notice to all users of the EndoWrist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice¿ Multifunction Electrode Part Number: MC171 OH Recalled by...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.