Alembic Pharmaceuticals Limited

Complete recall history across all FDA and CPSC categories — 7 total recalls

Alembic Pharmaceuticals Limited 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 (7)

FDA drug safety enforcement actions by Alembic Pharmaceuticals Limited

Date Product Reason Class
Dec 16, 2025 Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets, Rx only, M... Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impur... Class III
Oct 10, 2025 Fesoterodine Fumarate, Extended-release Tablets, 4 mg, 30-count bottle, Rx on... Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impur... Class III
Jul 25, 2025 Doxepin Hydrochloride Capsules, USP, 10 mg, 100 Capsules, Rx only, Manufactur... CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity abov... Class II
May 9, 2025 Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alemb... Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil ... Class II
May 7, 2025 Bromfenac Ophthalmic Solution 0.09%, 1.7 mL bottle, Rx only, Sterile, Manufac... Failed Impurities/Degradation Specifications Class II
Mar 17, 2021 Telmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: A... Labeling: Label-mixup Class I
Jun 10, 2020 Aripiprazole Tablets, USP, 2 mg, 30 Tablets per bottle, Rx only, Manufactured... Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had ar... 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.

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