LOW RISK
Terminated
F-0926-2020
CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
Recalled by Alfa Vitamins Laboratories, Inc.
Classification
Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.
Reason for Recall
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
Product Details
Product Quantity
1877 bottles
Product Type
Food
Code Info
LOT 31453 MFG 06 2019 EXP 06 2022
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Domestic distribution only.
Company Location
Miami, FL, 33166-5521
Timeline
Report Date
05/06/2020
Recall Initiated
03/24/2020
Classification Date
04/29/2020
Termination Date
08/25/2020
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 29, 2026
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