Rubicon Research Private Limited

Complete recall history across all FDA and CPSC categories — 4 total recalls

Rubicon Research Private 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 (4)

FDA drug safety enforcement actions by Rubicon Research Private Limited

Date Product Reason Class
Aug 24, 2024 AcetaZOLAMIDE Tablets, USP, 125 mg, 100 count bottled, Rx Only, Distributed b... Discoloration Class III
May 6, 2024 Metoprolol Tartrate Tablets USP, 25mg, 1000 count bottle, Rx only, distribute... Presence of Foreign Substance: metal in tablet Class II
Apr 26, 2024 traMADol Hydrochloride Tablets, USP 50 mg, 1000-count bottle, Rx Only, Distri... Presence of Foreign Tablets: Pharmacist reported a tablet of baclofen in a bo... Class II
Dec 31, 2021 Metoprolol Tartrate Tablets, USP 25 mg, 1000 - count bottle, Rx Only, Distrib... Complaint received of foreign matter (metal) embedded in tablet. 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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