Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported February 13, 2019
the silver bullet 10x Capsules, 725 mg each (proprietary blend of: Mucuna Pruriens Extract, Horny Goat Weed, Ginger Root Extract, Icariin, Wolf Berry (fruit) Lactase, Tribulus Terrestris Extract, Piperine), 10 count mylar package, Nature's Rx, Claremont, CA
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil
Natures Rx recalled the silver bullet 10x Capsules, 725 mg each (proprietary blend of: Mucuna Pruriens Extrac… - a critical-severity action.
the silver bullet 10x Capsules, 725 mg each (proprietary blend of: Mucuna Pruriens Extrac… was recalled by Natures Rx in February 13, 2019. Reason: Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil an…. Check the official notice for the remedy. Verify recall #D-0500-2019 with the FDA Drug before acting.
The recall
Natures Rx issued this critical-severity FDA Drug recall-Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil an….
- Critical
- severity level
- 211 units
- affected scope
- Class I
- classification
- February 13, 2019
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0500-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0500-2019) was formally reported on February 13, 2019, with the manufacturer initiating the action on January 25, 2019. It is classified under Critical severity (Class I), with a current status of Terminated. Natures Rx is listed as the recalling firm, operating out of Claremont, CA. Federal records list the affected scope as 211.
The documented reason for this recall is: Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil Distribution data in the federal record shows the product reached: eBay sales. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
211
Related Recalls
6
0 from same agency
Product description
the silver bullet 10x Capsules, 725 mg each (proprietary blend of: Mucuna Pruriens Extract, Horny Goat Weed, Ginger Root Extract, Icariin, Wolf Berry (fruit) Lactase, Tribulus Terrestris Extract, Piperine), 10 count mylar package, Nature's Rx, Claremont, CA
Reason for recall
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-0500-2019 |
| Date reported | February 13, 2019 |
| Date initiated | January 25, 2019 |
| Recalling firm | Natures Rx |
| Firm location | Claremont, CA |
| Affected scope | 211 |
| Distribution | eBay sales |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0500-2019) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
the silver bullet 10x Capsules, 725 mg each (proprietary blend of: Mucuna Pruriens Extract, Horny Goat Weed, Ginger Root Extract, Icariin, Wolf Berry (fruit) Lactase, Tribulus Terrestris Extract, Piperine), 10 count mylar package, Nature's Rx, Claremont, CA. Recalled by Natures Rx. Units affected: 211.
Why was this product recalled? ▼
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 13, 2019. Severity: Critical. Recall number: D-0500-2019.
Where was the recalled product distributed? ▼
Distribution: eBay sales.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0500-2019) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Conair Recalls Over One Million Cuisinart Grill Brushes Due… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported February 13, 2019. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.