Strides Pharma Inc.

Complete recall history across all FDA and CPSC categories — 8 total recalls

Strides Pharma 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 (8)

FDA drug safety enforcement actions by Strides Pharma Inc.

Date Product Reason Class
Dec 29, 2023 Methoxsalen Capsules, USP 10mg, 50-count bottle, Rx Only, Manufactured by: St... Failed Dissolution Specifications Class II
Jun 26, 2023 Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, ... Presence of Foreign Substance: Presence of a small piece of blue plastic embe... Class II
Jul 19, 2022 Prednisone Tablets USP, 20 mg, 100-count bottle, Rx Only, Manufactured by: St... Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone Tab... Class II
May 18, 2022 Losartan Potassium Tablets, USP 25 mg, Rx only, Manufactured by: Vivimed Lif... CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits Class II
May 18, 2022 Losartan Potassium Tablets, USP, 100 mg, Rx Only, Manufactured by: Vivimed Li... CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits Class II
May 18, 2022 Losartan Potassium Tablets, USP, 50 mg, Rx Only, Manufactured by: Vivimed Lif... CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits Class II
Sep 27, 2021 Potassium Chloride Extended-Release Tablets, USP 10 mEq (750 mg), 500 Tablets... Failed Dissolution Specifications Class II
Dec 22, 2020 NDC 64380-721-06 TACROLIMUS CAPSULES, USP 1mg 100 Capsules Rx Only Manufactur... Failed Moisture Limits 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.

Explore More Recalls

Search recalls by category, state, reason, or firm across all our databases.