Dietary Supplement Electro Buzz Recalled for Undeclared Active Pharmaceutical Ingredients
SAINI TRADE INC is recalling ELECTRO BUZZ dietary supplement (lot KT-1ST-43-01-07/2024, expiring 10/15/2026) distributed nationwide. Laboratory testing found undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
The agency’s classification
FDA (Drugs): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this as Class I, which mandates a minimum severity score of 4 per the rubric. Undeclared pharmaceutical ingredients in a dietary supplement marketed without approval present serious potential health risks.
Plain-English summary
SAINI TRADE INC is recalling ELECTRO BUZZ dietary supplement, 10 capsules per box (UPC B0DK68LF6J), distributed by Health Fixer, Tempe, AZ 85288. The affected lot is KT-1ST-43-01-07/2024 with expiration date 10/15/2026. Approximately 300 boxes were distributed nationwide.
Laboratory analysis found the product to be tainted with undeclared pharmaceutical ingredients: chloropretadalafil, propoxyphenylsildenafil, and sildenafil. The product was marketed without an Approved NDA/ANDA (New Drug Application/Abbreviated New Drug Application).
Consumers who have purchased this product should stop using it immediately. Consumers with questions or concerns about this recall should contact Health Fixer or speak with their healthcare provider.
The recalled product
- Product
- ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.
- Manufacturer
- SAINI TRADE INC
- Category
- Drug — Dietary Supplement
- Affected units
- 300
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- All lots Lot #: KT-1ST-43-01-07/2024
- Exp. 10/15/2026
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 5 recalled by SAINI TRADE INC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 5 products in this recall →Related recalls
Same manufacturer · SAINI TRADE INC
See all →- SevereMale Ultra Pro dietary supplement recalled for undeclared pharmaceutical ingredients
FDA (Drugs) · 2025-06-18
- SevereDietary Supplement ULTRA ARMOR Recalled for Undeclared Drug Ingredients
FDA (Drugs) · 2025-06-18
- SevereMALEXTRA Dietary Supplement Recalled for Undeclared Pharmaceutical Ingredients
FDA (Drugs) · 2025-06-18
- SevereDietary Supplement Male Ultra Recalled for Undeclared Drug Ingredients
FDA (Drugs) · 2025-06-18
Same hazard · undeclared active ingredient
See all →- SevereSupplement Capsules Recalled for Undeclared Sildenafil Content Nationwide
FDA (Drugs) · 2024-01-03
- SevereMegMan Performance Booster capsules recalled for undeclared tadalafil
FDA (Drugs) · 2022-02-16
- SevereThumbs Up 7 Red Capsules Recalled for Undeclared Active Pharmaceutical Ingredients
FDA (Drugs) · 2021-07-28
- SevereFDA Recalls PremierZen Platinum 5000 for Unapproved Active Ingredients
FDA (Drugs) · 2021-05-05
Similar recalls
- SevereZero Xtreme Dietary Supplement Recalled for Undeclared Sibutramine
FDA (Drugs) · 2018-11-21
- SevereDietary supplement found to contain undeclared pharmaceutical drug tadalafil
FDA (Drugs) · 2022-07-27
- CriticalBoost Ultra Supplement Recalled for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2014-05-28
- SevereDietary supplement Arize recalled for undeclared pharmaceutical ingredient
FDA (Drugs) · 2024-02-28
- CriticalDietary Supplement Recalled for Undeclared Sildenafil and Analogs
FDA (Drugs) · 2016-10-26
- CriticalFDA Recalls ZDaily Testosterone Supplement for Undeclared Prescription Drugs
FDA (Drugs) · 2017-07-19