Calci-Max Dietary Supplement Recalled for Zinc Content Deficiency
Alfa Vitamins Laboratories is recalling Calci-Max dietary supplements because FDA testing found the product contained 0.0% of the labeled zinc content.
The agency’s classification
FDA (Food): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which the rubric defines as typically resulting in a score of 1 or 2 because it is unlikely to cause adverse health consequences. The hazard is a labeling/quality discrepancy rather than a safety risk like contamination or injury.
Plain-English summary
Alfa Vitamins Laboratories, Inc. is recalling 1,877 bottles of CALCI-MAX Dietary Supplement, 60 capsules, manufactured for DOMEL. The recall is limited to Lot 31453, with a manufacture date of 06 2019 and an expiration date of 06 2022. The product was distributed domestically only.
The recall was initiated after FDA sample analysis showed that the zinc content of the affected lot was 0.0% of the label claim. This means the product does not contain the amount of zinc stated on the packaging.
Consumers who have this specific lot of Calci-Max should stop using the product and contact the recalling firm for further instructions or a refund. The recall is classified as Class III by the FDA, indicating that use of or exposure to the violative product is not likely to cause adverse health consequences.
The recalled product
- Product
- CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
- Manufacturer
- Alfa Vitamins Laboratories, Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,877
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- LOT 31453 MFG 06 2019 EXP 06 2022
Distribution
Distribution scope not specified by the agency.
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