CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
Recalling firm: Alfa Vitamins Laboratories, Inc.
Why it was recalled
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
The exact product
CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
LOT 31453 MFG 06 2019 EXP 06 2022
Recall details
- Recall number
- F-0926-2020
- Event ID
- 85317
- FDA status
- Terminated
- Initiated
- Mar 24, 2020
- Reported
- May 6, 2020
- Classified
- Apr 29, 2020
- Terminated
- Aug 25, 2020
- Quantity
- 1877 bottles
- Location
- Miami, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Domestic distribution only.
FDA source record · F-0926-2020
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.