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. 2,759 recalls have been distributed to Ohio in the last 12 months.
Showing 7901–7920 of 13,469 recalls
Recalled Item: Deferoxamine Mesylate for injection Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Firm failed to control impurity for color change at the API...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corporation Due to Lack...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corporation Due...
The Issue: Lack of Assurance of Sterility: Bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Argatroban Injection Recalled by Hospira Inc., A Pfizer Company Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...
The Issue: Lack of Assurance of Sterility: Customer complaints for leaking bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Oral Suspension Recalled by Precision Dose Inc. Due to...
The Issue: Labeling Error: Label mix-up. Products' unit dose cups are correctly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: D-ZINE Rapid Size and Strength capsules Recalled by HARDCORE FORMULATIONS...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA-STEN Rapid Size and Strength capsules Recalled by HARDCORE...
The Issue: Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...
The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...
The Issue: Presence of Foreign Substance: possibility of the presence of metal in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...
The Issue: Microbial contamination of non-sterile product: product failed Total...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 15 mMol in Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.