<a target=_blank class=ftalternatingbarlinklarge href="http://www.fda.gov/bbs/topics/enforce/2006/ENF00975.html
">http://www.fda.gov/bbs/topics/...ce/2006/ENF00975.html
</a>
PRODUCT
ADVAIR DISKUS® (fluticasone propionate/salmeterol inhalation powder), 250/50 mcg, 60-dose pack, Rx only, NDC 0173-0696-00, Recall # D-006-7
CODE
Lot: 6ZP3320, exp. 08/07
RECALLING FIRM/MANUFACTURER
GlaxoSmithKline Inc., Zebulon, NC, by letters beginning on September 19, 2006. Firm initiated recall is ongoing.
REASON
The Diskus unit may be defective resulting in medication not being dispensed as the doses are advanced.
VOLUME OF PRODUCT IN COMMERCE
22,530 units
DISTRIBUTION
Nationwide
">http://www.fda.gov/bbs/topics/...ce/2006/ENF00975.html
</a>
PRODUCT
ADVAIR DISKUS® (fluticasone propionate/salmeterol inhalation powder), 250/50 mcg, 60-dose pack, Rx only, NDC 0173-0696-00, Recall # D-006-7
CODE
Lot: 6ZP3320, exp. 08/07
RECALLING FIRM/MANUFACTURER
GlaxoSmithKline Inc., Zebulon, NC, by letters beginning on September 19, 2006. Firm initiated recall is ongoing.
REASON
The Diskus unit may be defective resulting in medication not being dispensed as the doses are advanced.
VOLUME OF PRODUCT IN COMMERCE
22,530 units
DISTRIBUTION
Nationwide