Risk Statement: Consumption of products with undeclared PDE-5 interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.
To date, HEALTH FIXER has not received any reports of adverse events related to this recall.
The products are used as an oral supplement and are packaged in blister packs containing 10 units of capsules, with the associated codes as follows:
Product Name |
NDC/UPC |
Lot Numbers |
Expiration |
---|---|---|---|
Male Ultra |
B0CMQ4FTHG |
KT-1ST-43-0110-2025 |
01/10/2027 |
Malextra |
B0CWKZ6ZP3 |
KT-1ST-43-0104/2026 |
04/25/2026 |
Electro Buzz |
B0DK68LF6J |
KT-1ST-43-0107/2024 |
10/15/2026 |
Ultra Armor |
B0CYJ7Y5H9 |
KT-1ST-43-0110/2025 |
01/10/2027 |
Male Ultra Pro |
B0CZN7C6YH |
KT-1ST-43-0110/2025 |
03/15/2026 |
Health Fixer’s supplements were distributed Nationwide across the U.S to Amazon Online Shopping.
HEALTH FIXER is notifying its distributors and customers by this press release of all Health Fixer’s recalled products. Consumers that have any Health Fixer dietary supplements which is being recalled should immediately stop using, discard any of the supplements and may contact their doctor in case of any health risk.
Consumers with questions regarding this recall can contact Health Fixer by the following number (414-888-8818) or e-mail ultrahelpbyfixer@gmail.com from Monday to Friday 9a.m. – 6p.m. Mountain time zone.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Complete and submit the report Online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178