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. 1,118 recalls have been distributed to Ohio in the last 12 months.
Showing 14261–14280 of 55,415 recalls
Recalled Item: FEM-PRIN MENSTRUAL RELIEF (acetaminophen 325 mg Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Multi Symptom Cold Relief (acetaminophen 325 mg Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAPENOL (acetaminophen 500 mg) Recalled by Ultra Seal Corporation Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Headache & Congestion Sinus Relief (acetaminophen 250 mg Recalled by Ultra...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAIN TERMINATOR extra strength pain relief (aspirin 162 mg Recalled by Ultra...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Away Pain Reliever/Fever Reducer (NSAID) (acetaminophen 110 mg Recalled...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sinus Relief Headache/Nasal (acetaminophen 325mg Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHLORESIN (acetaminophen 325mg Recalled by Ultra Seal Corporation Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Legatrin PM Pain Reliever/Sleep Aid (acetaminophen 500 mg Recalled by Ultra...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cold/Sinus Pain Reliever/Fever Reducer Nasal Decongestant (acetaminophen 325...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAINAID PMF Premenstrual Formula (acetaminophen 500 mg Recalled by Ultra...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MidNite Sleep Health (melatonin 1.5 mg) tablets Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nutralox Mint Antacid (calcium carbonate 420mg) Chewable tablets Recalled by...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PAINAID (acetaminophen 110 mg Recalled by Ultra Seal Corporation Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CONGESTAID II Nasal Decongestant (Phenylephrine HCl 5mg) 2 tablet packets...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite Remfresh Advanced Ion-Powered Melatonin (Melatonin 0.5mg) Tablets...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proctofoam HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%)...
The Issue: cGMP deficiencies
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1. Footrest ( use exclusively in combination with Intelli-C devices)...
The Issue: Friction rubber block in the clamping mechanism was missing in the Footrest....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.