Why it was recalled
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
Product description
CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
Lot numbers, UPCs & expiration codes
LOT 31453 MFG 06 2019 EXP 06 2022
Where it was sold
Domestic distribution only.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0926-2020
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Mar 24, 2020
- FDA report date
- May 6, 2020
- Quantity
- 1877 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Alfa Vitamins Laboratories, Inc.
Original FDA data
Every field from FDA enforcement report F-0926-2020, exactly as published.
Show all FDA fields
- City
- Miami
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 85317
- Address
- 4701 NW 77th Ave
- Code information
- LOT 31453 MFG 06 2019 EXP 06 2022
- Postal code
- 33166-5521
- Report date
- May 6, 2020
- Product type
- Food
- Recall number
- F-0926-2020
- Classification
- Class III
- Recalling firm
- Alfa Vitamins Laboratories, Inc.
- Product quantity
- 1877 bottles
- Termination date
- Aug 25, 2020
- Reason for recall
- FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
- Distribution pattern
- Domestic distribution only.
- Recall initiation date
- Mar 24, 2020
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Apr 29, 2020