Macleods Pharma Usa, Inc

Complete recall history across all FDA and CPSC categories — 6 total recalls

Macleods Pharma Usa, 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 (6)

FDA drug safety enforcement actions by Macleods Pharma Usa, Inc

Date Product Reason Class
Feb 26, 2026 Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manuf... Subpotent Drug Class II
May 7, 2024 Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-c... Presence of foreign substance: plastic-like substance. Class II
Jan 5, 2023 Levofloxacin Tablets, USP 500 mg; 50-count bottles, Rx Only, Manufactured for... Mismatching of the embossing on the tablets (T7) with the embossing mentioned... Class III
Oct 18, 2021 Rizatriptan Benzoate Orally Disintegrating Tablets 5mg, 12 Tablets (2 x 6 Uni... Out-of-specification test results obtained in Organic Impurities test during ... Class III
Oct 18, 2021 Rizatriptan Benzoate Orally Disintegrating Tablets 10mg, 18 Tablets (3 x 6 Un... Out-of-specification test results obtained in Organic Impurities test during ... Class III
Oct 18, 2021 Rizatriptan Benzoate Film Coated Tablets, 10 mg, packaged in a) 12 Tablets (2... Out-of-specification test results obtained in Organic Impurities test during ... 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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