FDA INFORMS PUBLIC OF NATIONWIDE INFANT FORMULA
RECALL

The U.S. Food and Drug
Administration (FDA) is alerting the public to a recall being conducted by Mead
Johnson for their GENTLEASE powdered infant formula, lot number: BMJ19, use by 1
Jul 07. This lot was found to contain metal particles, consisting of up to 2.7
millimeter in size.

No illnesses have
been reported to date. However, in the rare instance that an infant were to
inhale the infant formula into the lungs, the presence of these particles could
present a serious risk to the infant’s respiratory system and throat. Any
injuries associated with this problem would be likely to show up within three to
four hours. The symptoms could be varied depending on whether there is damage
to the throat or lungs. Damage to the throat may include coughing, difficulty
swallowing or difficulty breathing. Similarly damage to the lungs could include
coughing and difficulty breathing. If you may have fed this lot of GENTLEASE to
your baby, and you have any concerns about your baby’s health, you should
contact your baby’s health professional for guidance.

There were approximately 41,464
24-ounce cans of this lot of recalled product distributed, beginning on December
16, 2005, through many major retail stores across the country, so the consumer
should concentrate on the code on the can rather than on the place of purchase.
The affected products can be identified by the lot number and expiration/use by
date embossed on the bottom of the can of BMJ19, use by 1 Jul 07.

Mead Johnson informed the FDA of this
problem. FDA and Mead Johnson are currently investigating the cause of the
metal particles found in the infant formula in this highly unusual
incident.

Consumers who have a can of
this batch of GENTLEASE powdered infant formula should not use the product and
should contact Mead Johnson at 888-587-7275 immediately.