ANNOUNCED ONGOING Food recall · Reported 4 Sep 2026 · FDA company announcement, classification pending
Business Pill, Branch Manager recalled by Supplx.com
Supplx.com is recalling Business Pill, Branch Manager for Men dietary supplements marketed for male sexual. The recall was initiated on 3 Sep 2026 and is listed as ongoing.
Recall details
- Recall number
- FDA-PR-f8f950b8c510
- Recalling firm
- Supplx.com
- Classification
- Pending
- Status
- Ongoing
- Recall initiated
- 3 Sep 2026
- Reported
- 4 Sep 2026
- Reason category
- Undeclared Allergens
- Product category
- Sexual Enhancement Products
Timeline
| 3 Sep 2026 | Recall initiated by company | |
| 4 Sep 2026 | Published in enforcement report | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Products contain undeclared yohimbine. 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. Yohimbine is a plant-derived alkaloid formulated for use as a prescription medication, generally as a treatment for erectile dysfunction. It has also been studied for use to promote blood flow and support athletic performance. FDA found dangerously high levels of yohimbine in the recalled products. Yohimbine can cause severe hypertension, tachycardia, and possibly cardiac arrhythmia and myocardial infarction (heart attacks), especially if the consumer is taking other stimulants such as caffeine or ephedra-containing products or prescription drugs used to treat ADHD. Severe gastrointestinal distress, including nausea, vomiting, diarrhea and stomach pain are typical side effects of high doses. It can also cause acute neurologic and psychiatric effects, including anxiety, insomnia, mania, psychosis in schizophrenic patients, drowsiness, disorientation, tremors and seizures. Death has been reported in cases of severe overdose. The recalled products were packaged in single-capsule blister cards and sold in 24-count retail boxes through SUPPLX.com. The recall covers all lots and expiration or best-by dates distributed from September 16, 2023, through June 11, 2026. Lot and expiration or bes
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the company
Business Pill, Branch Manager for Men dietary supplements marketed for male sexual enhancement
Where it was distributed
Not stated.
Questions about this recall
Why was it recalled?
Products contain undeclared yohimbine. 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. Yohimbine is a plant-derived alkaloid formulated for use as a prescription medication, generally as a treatment for erectile dysfunction. It has also been studied for use to promote blood flow and support athletic performance. FDA found dangerously high levels of yohimbine in the recalled products. Yohimbine can cause severe hypertension, tachycardia, and possibly cardiac arrhythmia and myocardial infarction (heart attacks), especially if the consumer is taking other stimulants such as caffeine or ephedra-containing products or prescription drugs used to treat ADHD. Severe gastrointestinal distress, including nausea, vomiting, diarrhea and stomach pain are typical side effects of high doses. It can also cause acute neurologic and psychiatric effects, including anxiety, insomnia, mania, psychosis in schizophrenic patients, drowsiness, disorientation, tremors and seizures. Death has been reported in cases of severe overdose. The recalled products were packaged in single-capsule blister cards and sold in 24-count retail boxes through SUPPLX.com. The recall covers all lots and expiration or best-by dates distributed from September 16, 2023, through June 11, 2026. Lot and expiration or bes
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does an unclassified recall mean?
The FDA assigns a class once it has assessed the health risk. Until then the recall is listed without one.
Read the official FDA notice · Source record retrieved 26 Sep 2026. This is a company announcement published by the FDA; the FDA has not yet classified the recall. The record is updated when the classification appears in the Enforcement Report. This page reports the record and gives no medical advice.
Other Sexual Enhancement Products recalls
All 9| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | ANNOUNCED | X10 Natural Enhancement Supplement recalled by A&P CreationsX10 | A&P Creations | Hidden Drug Ingredients | |
| Food | ANNOUNCED | biQ-FEL supplement recalled by A&P CreationsbiQ-FEL | A&P Creations | Hidden Drug Ingredients | |
| Food | CLASS II | Pure Libido Drink recalled by Liquid Blenz | Liquid Blenz | Botulism | NY |
| Food | CLASS I | Boner Bears Honey Male Enhancement 100% Wildflower Honey recalledBoner Bears | Pure Vitamins and Natural Supplements | Undeclared Allergens | NJ |
| Food | CLASS I | Red Bull Extreme Male Enhancement Supplement recalled | Pure Vitamins and Natural Supplements | Undeclared Allergens | NJ |