May 24, 2000SmithKline Beecham Recalls
Feosol(r) Elixir Iron Supplement Therapy
NY (SafetyAlerts) - The Food and
Drug Administration (FDA) today reported that SmithKline Beecham Consumer Healthcare is
conducting a recall of Feosol(r) Elixir Iron Supplement Therapy 44mg, in 16-ounce (473ml)
bottles, because of subpotent iron content (stability testing) and crystalline
The recalled Feosol(r) bear the Lot
Numbers 9H23A and 9J11A. FDA stated in it's report that 884 cases were distributed
This ongoing Class II recall
was initiated by the company, by letter and public warning on February 18, 2000.
This is the first public notice issued by the FDA.
Questions concerning this recall may
be directed to the FDA at 1-888-INFO-FDA.
FDA Recall #d-347-0
Notice of this product warning was
sent via email to SafeMail
subscribers May 24, 2000.
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