Organic Herbal Supply
Complete recall history across all FDA and CPSC categories — 12 total recalls
Organic Herbal Supply 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 (12)
FDA drug safety enforcement actions by Organic Herbal Supply
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 18, 2017 | BIGnHARD Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, suppli... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | ZRECT for Women Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 co... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | TORNADO Male Enhancement Herbal Dietary Supplement Capsules, Over 4000 mg val... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | ZRECT Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied i... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules, suppl... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | LabidaMAX Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count pa... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | RECTALIS Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplie... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | Cummor Natural Male Enhancement, Herbal Dietary Supplement Capsules, 500 mg, ... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | ENHANCEROL Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 1... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | Xrect Male Enhancement Herbal Dietary Supplement Capsules, 500 mg supplied in... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Apr 18, 2017 | ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement Capsu... | Marketed without an Approved NDA/ANDA; FDA analysis found the presence of und... | Class I |
| Feb 16, 2017 | XtraHRD Natural Male Enhancement Capsules, Herbal Dietary Supplement, 500 mg ... | Marketed without an Approved NDA/ANDA: Product contains N-desmethyl tadalafil... | Class I |
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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