Bulk tablet label
Reason Product contains higher levels of niacin than claimed on label .
KEYTABS (Without Iron recall
Recalled by Ancient Formulas Inc · Wichita, KS, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains higher levels of niacin than claimed on label .
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
KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product of The Key Company, St. Louis, MO.
Quantity: 124/180-tablet bottles
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 YDBI, Exp. 03/2016
Where it was sold
Missouri
FDA's distribution note: The bulk tablets were distributed to MO where they were repackaged into bottles. There was no foreign/military/government distribution.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Ancient Formulas Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 22, 2013
- In FDA report of
- Aug 21, 2013
- Terminated
- Aug 12, 2013
- FDA recall number
- F-1803-2013 · event 64764
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
Other recalls by Ancient Formulas Inc
Healthprint Vitamin D3 5000 Dietary Supplement
Reason Product is sub-potent for Vitamin D and label contains incorrect percent daily value.