West-Ward Columbus Inc

Complete recall history across all FDA and CPSC categories — 9 total recalls

West-Ward Columbus 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 (9)

FDA drug safety enforcement actions by West-Ward Columbus Inc

Date Product Reason Class
Dec 19, 2024 Methadone Hydrochloride Tablets, USP, 5mg, 10x10 Unit-Dose Tablets, Rx Only, ... Failed Tablet/Capsule Specifications: Illegible product identification for th... Class III
Sep 22, 2023 Methotrexate Tablets, USP, 2.5 mg, 10x10 Unit-Dose Tablets per carton, Rx onl... Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmoo... Class III
Jul 22, 2020 Leucovorin Calcium Tablets USP, 10 mg, Rx only, 24 Tablets per bottle, Distr.... Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrec... Class III
May 13, 2020 Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. b... Failed Impurities/Degradation Specifications: Out of Specification for impuri... Class III
May 13, 2020 Doxycycline Hyclate Tablets USP, 100 mg, packaged in a) 50-count bottle (NDC ... Failed dissolution specification: The dissolution test at the 24 month time p... Class II
Sep 9, 2019 Oxcarbazepine Oral Suspension, USP, 300 mg/5 mL, 250 mL per bottle, Rx Only, ... Failed Impurities/Degradation Specificattion Class II
Jul 24, 2018 Doxycycline Hyclate Tablets, USP, 100 mg*. 50-count bottle, Rx only. Manufact... Failed Dissolution Specifications: Class II
Jul 24, 2018 Doxycycline Hyclate Tablets, USP, 100 mg*. 500-count bottle, Rx only. Manufac... Failed Dissolution Specifications: Class II
May 19, 2016 Oxycodone HCl, Oral Solution USP, 5 mg/5 mL, 15 mL bottles, Rx only, Boehring... Failed Impurities/Degradation Specification; 9 month stability Class III

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.

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