Food Recall Check
Class III · Low risk Terminated Initiated Mar 24, 2020 (7 years ago)

CALCI-MAX Dietary Supplement recall

Recalled by Alfa Vitamins Laboratories, Inc. · Miami, FL, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL

Quantity: 1877 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

LOT 31453 MFG 06 2019 EXP 06 2022

Where it was sold

FDA's distribution note: Domestic distribution only.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Alfa Vitamins Laboratories, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 24, 2020
In FDA report of
May 6, 2020
Terminated
Aug 25, 2020
FDA recall number
F-0926-2020 · event 85317
Official record
FDA enforcement report search

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