CALCI-MAX Dietary Supplement — Class III food recall F-0926-2020
Terminated recall by Alfa Vitamins Laboratories, Inc., reported 2020-05-06. FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
| Recall number | F-0926-2020 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Alfa Vitamins Laboratories, Inc., Miami, FL, United States |
| Recall initiated | 2020-03-24 |
| Classified | 2020-04-29 |
| Reported by FDA | 2020-05-06 |
| Terminated | 2020-08-25 |
| Quantity | 1,877 bottles |
| Reason classes | labeling |
| Lot numbers | 2019, 2022, 31453 |
Product
CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
Reason for recall
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
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/F-0926-2020. 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.