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. 2,757 recalls have been distributed to Ohio in the last 12 months.
Showing 10361–10380 of 55,415 recalls
Recalled Item: FURIKAKE SEASONED ROASTED SEAWEED FLAKES SPICY Product #38246 Brand name:...
The Issue: Product was found to have the incorrect crustacean named on products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FURIKAKE SEASONED ROASTED SEAWEED FLAKES SEAFOOD Product number: 38245 Brand...
The Issue: Product was found to have the incorrect crustacean named on products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gerber GoodStart SoothePro Infant Formula with Iron. Milk Based Powder....
The Issue: Infant Formula has the potential to be contaminated with Cronobacter spp.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...
The Issue: CGMP Deviations: recalling drug products following an FDA inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...
The Issue: CGMP Deviations: recalling drug products following an FDA inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Out of...
The Issue: Out of specification (OOS) for Spectroscopic Identification test by IR.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...
The Issue: CGMP Deviations: recalling drug products following an FDA inspection.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...
The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SenSight Extension Tunneler Kit Recalled by Medtronic...
The Issue: Medtronic has received reports of SenSight Extension Tunneler kits that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery....
The Issue: Device suddenly and forcefully disassembled after cryotherapy, potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...
The Issue: Light handle covers may separate from the light handle (detach and fall off)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Cortisol 50T (Material Number 10994924) Recalled by Siemens...
The Issue: There is a negative bias with urine patient samples and urine cortisol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integre Pro Yellow LP561 Recalled by Ellex Medical Pty Ltd. Due to When...
The Issue: When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JULIET Ti LL Recalled by SPINEART SA Due to JULIET Lateral Lumbar Ti-Life...
The Issue: JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Cortisol 50T (Material Number 10995538) Recalled by Siemens...
The Issue: There is a negative bias with urine patient samples and urine cortisol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Carefusion V. Mueller Graves Vaginal Speculum Recalled by Carefusion...
The Issue: A portion of the two products were incorrectly marked (etched) and packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doxazosin Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glimepiride Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tadalafil Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.