MegaJex Herbal Supplement — Class I drug recall D-0472-2017
Terminated recall by MS Bionic, reported 2017-02-22, distributed in CA. Marketed without an Approved NDA/ANDA; product contains sildenafil and tadalafil which are active pharmaceutic
| Recall number | D-0472-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MS Bionic, Gardena, CA, United States |
| Recall initiated | 2016-11-30 |
| Classified | 2017-02-13 |
| Reported by FDA | 2017-02-22 |
| Terminated | 2017-06-01 |
| Distributed | CA |
| Quantity | 100 bottles |
| Reason classes | unapproved product |
| Expiration dates | 2019-12 |
Product
MegaJex Herbal Supplement, Maximum Formula for Men, Fast acting, Increase Stamina, 20 capsules, MS Bionics, Gardena, CA
Reason for recall
Marketed without an Approved NDA/ANDA; product contains sildenafil and tadalafil which are active pharmaceutical ingredients in FDA approved drugs used to treat erectile dysfunction (ED)
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0472-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.