Ohm Laboratories, Inc.

Complete recall history across all FDA and CPSC categories — 23 total recalls

Ohm Laboratories, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (23)

FDA drug safety enforcement actions by Ohm Laboratories, Inc.

Date Product Reason Class
Jul 28, 2015 Premier Value Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count ... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Equaline Original Prescription Strength, loratadine orally disintegrating tab... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Rite Aid Pharmacy loratadine orally disintegrating tablets USP, 10 mg, packag... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 CVS Pharmacy, Original Prescription Strength, LORATADINE ORALLY DISINTEGRATIN... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Up&Up loratadine orally disintegrating tablets, USP, 10 mg, 30-count tablets ... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Good Neighbor Pharmacy Loratadine Orally Disintegrating Tablets, USP, 10 mg, ... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Major loratadine orally disintegrating tablets, USP, 10 mg, 10-count tablets ... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Health Best Choice Care, Loratadine Orally Disintegrating Tablets, USP, 10 mg... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 QC Quality Choice Loratadine Orally Disintegrating Tablets, USP 10 mg, 10-cou... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 CareOne Original Prescription Strength, Allergy Relief, Loratadine Orally Dis... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Fred's Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-counts tablet... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Wal-itin Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a)... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Meijer Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 HEB Loratadine Orally Disintegrating Tablets, USP, 10 mg, 10-count tablets pe... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Discount Drug Mart Food Fair, Original Prescription Strength, Loratadine Oral... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Ohm Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets, D... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Health Mart Pharmacy loratadine orally disintegrating tablets, USP, 10 mg, 10... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 TopCare LORATIDINE ORALLY DISINTEGRATING TABLETS, , USP, 10 mg, packaged in a... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Safeway Care Loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged i... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Sunmark loratadine Orally Disintegrating Tablets, USP, 10 mg, packaged in a) ... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Jul 28, 2015 Leader Loratadine Orally Disintegrating Tablets, USP, 10 mg, 30-count tablets... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
May 4, 2015 Loratadine Orally Disintegrating Tablets USP, 10 mg, Antihistamine, Allergy R... Superpotent Drug: Out Of Specification (OOS) result for Assay. Class III
Feb 7, 2014 Non-Drowsy 24 Hour Formula Allergy Relief and Nasal Decongestant, Pseudoephed... Defective Container: An unacceptable level of blister defects have been ident... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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