SUPPLX.com Issues Voluntary Nationwide Recall of Business Pill and Branch Manager for Men Due to Undeclared Yohimbine
United States
Status not reported
- Product
- SUPPLX.com Issues Voluntary Nationwide Recall of Business P…
- Source
- FDA
Reason for recall
Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| SUPPLX.com Issues Voluntary Nationwide Recall of Business Pill and Branch Manager for Men Due to Undeclared Yohimbine | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution area was not published in this source record.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Safety Recalls (RSS)
- Recall number
- http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/supplxcom-issues-voluntary-nationwide-recall-business-pill-and-branch-manager-men-due-undeclared
- Status
- Not published in this source record
- Classification
- Not yet classified
- Company
- Not published in this source record
- Product description
- SUPPLX.com Issues Voluntary Nationwide Recall of Business Pill and Branch Manager for Men Due to Undeclared Yohimbine
- Quantity
- Not published in this source record
- Reason
- Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.
- Recall initiation date
- Not published in this source record
- Report date
- September 3, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Not published in this source record
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Where this information comes from
View public notice -- the original notice published by FDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a recall classification mean?
The agency has not yet assigned a recall classification.
Is this recall still active?
According to FDA, this recall's status is "not yet published." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
