Severity
Moderate
FDA Food recall · Reported August 21, 2013
Product contains higher levels of niacin than claimed on label .
Ancient Formulas Inc recalled KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product o… - a moderate-severity action.
KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product o… was recalled by Ancient Formulas Inc in August 21, 2013. Reason: Product contains higher levels of niacin than claimed on label .. Check the official notice for the remedy. Verify recall #F-1803-2013 with the FDA Food before acting.
The recall
Ancient Formulas Inc issued this moderate-severity FDA Food recall-Product contains higher levels of niacin than claimed on label ..
Sourced from official FDA Food enforcement records. Verify recall #F-1803-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1803-2013) was formally reported on August 21, 2013, with the manufacturer initiating the action on March 22, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Ancient Formulas Inc is listed as the recalling firm, operating out of Wichita, KS. Federal records list the affected scope as 124/180-tablet bottles.
The documented reason for this recall is: Product contains higher levels of niacin than claimed on label . Distribution data in the federal record shows the product reached: The bulk tablets were distributed to MO where they were repackaged into bottles. There was no foreign/military/government distribution.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 1 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
124/180-tablet bottles
Related Recalls
6
1 from same agency
KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product of The Key Company, St. Louis, MO.
Product contains higher levels of niacin than claimed on label .
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1803-2013 |
| Date reported | August 21, 2013 |
| Date initiated | March 22, 2013 |
| Recalling firm | Ancient Formulas Inc |
| Firm location | Wichita, KS |
| Affected scope | 124/180-tablet bottles |
| Distribution | The bulk tablets were distributed to MO where they were repackaged into bottles. There was no foreign/military/government distribution. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
AbbVie Inc. · 2026-06-03
Llorens Pharmaceuticals International Division, Inc. · 2026-05-27
Safecor Health, LLC · 2026-05-27
IntegraDose Compounding Services LLC · 2026-05-27
Lupin Pharmaceuticals Inc. · 2026-05-27
Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported August 21, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.