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Medical Supply Liquidators Llc

Complete recall history across all FDA and CPSC categories — 15 total recalls

Medical Supply Liquidators 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 (15)

FDA drug safety enforcement actions by Medical Supply Liquidators Llc

Date Product Reason Class
Jun 25, 2014 Lipo 8 Injection USP 200 mg/ml, packaged in 30 ml vials, Sterile, Manufacture... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Vitamin B6 Pyridoxine HCL for Injection USP, 100 mg/ml, Sterile, for IM or D... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Vitamin B12 Cyanocobalamin with MIC Injection USP 1000 mcg/ml, packaged in 10... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Vitamin B12 Methylcobalamin with MIC Injection USP 1000 mcg/ml, Sterile, 10 m... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Vitamin B12 Cyanocobalamin Injection USP 1000 mcg/ml, Sterile, 10 ml vial and... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 MIC Injection USP, Sterile, 10 ml vial and 30 ml vial, For IM or Deep SQ Use,... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 B Complex for Injection USP with Methylcobalamin 1000 mcg/ml, Sterile, for IM... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Vitamin B12 Methylcobalamin Injection USP 1000 mcg/ml, Sterile, 10 ml vial an... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Super MIC B Complex for L-Carnitine for Injection USP with Methylcobalamin 10... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 L-Carnitine Injection USP 100 mg/ml, packaged in 30 ml vials, Sterile, For IM... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Vitamin B12 Methylcobalamin 5000 Injection USP 5000 mcg/ml, 10 ml vial and 30... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Glutathione Injection USP, 200 mg/ml, packaged in 30 ml vials, Sterile, For I... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 BCAA 4% Branched Chain Amino Acid Injection USP, Sterile, 30 ml vial, For IM ... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 Vitamin B12 Hydroxocobalamin Injection USP 1000 mcg/ml, Sterile, 30 ml vial, ... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... Class II
Jun 25, 2014 G.A.C. 375 Injection USP, packaged in 30 ml vials, Sterile, For IM or Deep SQ... Marketed without an Approved NDA/ANDA; IM and SQ injectable products are bein... 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.

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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