Murray International Trading Co., Inc.
Complete recall history across all FDA and CPSC categories — 15 total recalls
Recall Summary
Murray International Trading Co., Inc. appears in recall records across 2 categories. 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.
Food Recalls (1)
FDA food safety enforcement actions by Murray International Trading Co., Inc.
| Date | Product | Reason | Class |
|---|---|---|---|
| Nov 2, 2021 | "Herbal Doctor" brand Angelicae Sinensis, Natural Herb, Net Wt. 16 oz (454 g)... | Product contains elevated levels of lead and cadmium | Class II |
Drug Recalls (14)
FDA drug safety enforcement actions by Murray International Trading Co., Inc.
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 20, 2016 | SCIATICA PILLS, packaged in 120-count bottles within a box, Made in the Peopl... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | Te Xiao BaiNeiTing Herbal Supplement (Naphazoline HCl Solution 0.1%) liquid, ... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | PING ON OINTMENT RELIEF FOR MUSCULAR PAIN, packaged in a packet of 12-count 8... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | WUPOOSER KAI YEUNG PILL, packaged in a bottle within a box, Made in The Peopl... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | LARYNGITIS PILLS Herbal Supplement, packaged in 10-count packets containing 3... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | ChingChunBao ANTI-AGING TABLETS, packaged in 80-count bottles within a box, U... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | PATCH-REMOUING PILL (For Facial Pigmentation), packaged in a bottle within a ... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | PEKING NIU-HUANG CHIEH-TU-PIEN Tablets (Sugar Coated), packaged in 50-count b... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | Tien Ma Tou Tong Wan (Condensed pills), packaged in 100-count bottles within ... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | CROCODILE BILE PILL FOR ASTHMA, packaged in 100-count bottles within a box, r... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | GASTRODIA CAPSULES, packaged in 30-count bottles within a box, LANZHOU MANUFA... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | FUQINGSONG RELIEF CREAM (Flucinonide Ointment), packaged in 50-count individu... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | FUCONPO CAPSULE, packaged in a 30-count bottle within a box, remaining labeli... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | Class II |
| Apr 20, 2016 | FARSER KAI YEUNG PILL, packaged in a bottle within a box, Made in The People... | Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements... | 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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