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FDA recall record

KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product of The Key Company, St. Louis, MO.

Recall F-1803-2013Class IITerminatedMarch 22, 2013

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of August 12, 2013. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product of The Key Company, St. Louis, MO.

Reason

Product contains higher levels of niacin than claimed on label .

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product of The Key Company, St. Louis, MO.

Code information listed by FDA

Lot YDBI, Exp. 03/2016

Distribution and firm information

Recalling firm listed by FDA: Ancient Formulas Inc

Firm location listed by FDA: Wichita, KS, United States

Distribution reported by FDA: The bulk tablets were distributed to MO where they were repackaged into bottles. There was no foreign/military/government distribution.

Product quantity listed by FDA: 124/180-tablet bottles

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.