Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported August 10, 2022
SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800) 519-0204 Miami 33172 FL, USA; UPC 0 705632 523285
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil.
Distributor Rfr, LLC. recalled SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carto… - a critical-severity action.
SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carto… was recalled by Distributor Rfr, LLC. in August 10, 2022. Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil.. Check the official notice for the remedy. Verify recall #D-1333-2022 with the FDA Drug before acting.
The recall
Distributor Rfr, LLC. issued this critical-severity FDA Drug recall-Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil..
- Critical
- severity level
- Class I
- classification
- August 10, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1333-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1333-2022) was formally reported on August 10, 2022, with the manufacturer initiating the action on July 22, 2022. It is classified under Critical severity (Class I), with a current status of Terminated. Distributor Rfr, LLC. is listed as the recalling firm, operating out of Doral, FL. Federal records list the affected scope as 2000 cartons.
The documented reason for this recall is: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil. Distribution data in the federal record shows the product reached: Retail stores in the state of FL, Nationwide in the USA, France and Canada via website sales, and Bolivarian Republic of Venezuela. 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.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements 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
2000 cartons
Related Recalls
6
0 from same agency
Product description
SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800) 519-0204 Miami 33172 FL, USA; UPC 0 705632 523285
Reason for recall
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-1333-2022 |
| Date reported | August 10, 2022 |
| Date initiated | July 22, 2022 |
| Recalling firm | Distributor Rfr, LLC. |
| Firm location | Doral, FL |
| Affected scope | 2000 cartons |
| Distribution | Retail stores in the state of FL, Nationwide in the USA, France and Canada via website sales, and Bolivarian Republic of Venezuela |
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-1333-2022) 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? ▼
SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800) 519-0204 Miami 33172 FL, USA; UPC 0 705632 523285. Recalled by Distributor Rfr, LLC.. Units affected: 2000 cartons.
Why was this product recalled? ▼
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 10, 2022. Severity: Critical. Recall number: D-1333-2022.
Where was the recalled product distributed? ▼
Distribution: Retail stores in the state of FL, Nationwide in the USA, France and Canada via website sales, and Bolivarian Republic of Venezuela.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1333-2022) 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 Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
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 August 10, 2022. 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.