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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 85317

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 24, 2020
Product types
Food
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Alfa Vitamins Laboratories, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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

F-0926-2020
Recall number
F-0926-2020
Initiated
March 24, 2020
Classification
Class III
Status
Terminated
Quantity
1877 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

LOT 31453 MFG 06 2019 EXP 06 2022

Distribution pattern

Domestic distribution only.