Legacy Pharmaceutical Packaging LLC

Complete recall history across all FDA and CPSC categories — 10 total recalls

Legacy Pharmaceutical Packaging LLC 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 (10)

FDA drug safety enforcement actions by Legacy Pharmaceutical Packaging LLC

Date Product Reason Class
Dec 11, 2023 Sertraline Tablets, USP 100 mg, 30 tablets per bottle, Distributed by: Wal-Ma... CGMP Deviations: Inadequate line clearance which may result in a potential co... Class II
Sep 24, 2020 Metformin Hydrochloride Tablets USP, 1000 mg, 60-count bottles, Rx Only, Man... Presence of Foreign Tablets/Capsules: Metformin 1000mg with different imprint... Class III
Apr 24, 2019 Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distribut... CGMP Deviations: Detection of trace amounts of N-Methylnitrosobutyric acid (N... Class II
Mar 1, 2019 Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distribut... CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) ... Class II
Mar 1, 2019 Losartan Potassium Tablets, USP, 25 mg, 30 tablet bottles, Rx Only, Distribut... CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) ... Class II
Mar 1, 2019 Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distribut... CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) ... Class II
Mar 1, 2019 Losartan Potassium Tablets, USP, 100 mg, 30 tablet bottles, Rx Only, Distrib... CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) ... Class II
Mar 7, 2017 ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The K... Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of ate... Class II
Apr 22, 2013 Walmart Amlodipine Besylate Tablets, USP 10 mg, Rx only, 30 tablets, Manufact... Labeling: Label Error on Declared Strength-The recalled product has a misprin... Class II
Mar 27, 2013 Lorazepam, 0.5 mg tablets, 100 count, RX only, Distributed by Major Pharmaceu... Labeling: Incorrect or Missing Lot and/or Exp Date: Lorazepam Lot # L-04009 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.

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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