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. 2,786 recalls have been distributed to Ohio in the last 12 months.
Showing 4381–4400 of 13,469 recalls
Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...
The Issue: Subpotent Drug: FDA analysis found product to be subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...
The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Strides Pharma Inc.Potassium Chloride Extended-Release Tablets Recalled by...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...
The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Sub-Potent Drug: Out of specification test results for potency (below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Teva Pharmaceuticals USA Due to...
The Issue: CGMP deviations; there is a possibility that some bottles in these lots may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by BAYSHORE...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amiodarone Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tranexamic Acid Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Goldenseal Root Powder Organic Recalled by Maison Terre, LLC Due to...
The Issue: Microbial Contamination of Non-Sterile Products: FDA laboratory analysis...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: CGMP Deviations: All other lots are being recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%) Recalled by...
The Issue: Chemical Contamination: FDA analysis found the product contains methanol,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Recalled by...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump Recalled...
The Issue: Marketed without an Approved NDA/ANDA; product labeled to contain 0.56%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine HCl Injection Recalled by Hikma Pharmaceuticals USA Inc. Due...
The Issue: Sub-potent Drug: Out-of-Specification assay results found at 3 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elitek (rasburicase) for injection Recalled by Sanofi-Aventis U.S. LLC Due...
The Issue: Failed Stability Specifications: Out of Specification result for enzyme...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisone Tablets Recalled by Lannett Company, Inc. Due to Labeling: Label...
The Issue: Labeling: Label Mix Up: bottle labeled to contain Prednisone Tablets, USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.