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. 2,580 recalls have been distributed to Ohio in the last 12 months.
Showing 28901–28920 of 55,415 recalls
Recalled Item: Diclofenac Sodium USP for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tramadol HCl USP (CIV) for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Celecoxib USP for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxandrolone USP for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Hemihydrate USP (Micronized) (Soy) for prescription compounding...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liothyronine Sodium USP for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentolamine Mesylate USP for prescription compounding Recalled by American...
The Issue: CGMP Deviations: Lack of stability data and controls to support the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kratom capsules labeled in the following ways: 1) Divinity Kratom Recalled...
The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kratom powder labeled in the following ways 1) Enhance Your Life Recalled by...
The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product packaged in the following ways A) Sonne's Recalled by Vitalab Co Inc...
The Issue: The firm's vitamin C dietary supplement contains lactose, a milk-derived...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM...
The Issue: Data has shown that degradation of a raw material used in Phantom Fiber may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 - Model no. 728231 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT - Model no. 728306 Computed Tomography X-Ray system Recalled...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT - Model no. 728326 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Flex - Model no. 728317 Recalled by Philips Medical Systems...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...
The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 6 Slice (Air) - Model no. 728256 Recalled by Philips Medical...
The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.