Product description
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.
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- Event ID
- 85317
- Code info
- LOT 31453 MFG 06 2019 EXP 06 2022
- Product quantity
- 1877 bottles
- Distribution pattern
- Domestic distribution only.
- Voluntary / mandated
- Voluntary: Firm initiated
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product type
- Food
- Recalling firm location
- 4701 NW 77th Ave, N/A, Miami, FL, United States
- Recall initiation date
- 03/24/2020
- Center classification date
- 04/29/2020
- Termination date
- 08/25/2020