July 11, 2002
Astrazeneca Has Recalled Pulmicort Turbuhaler
- The Food and Drug Administration (FDA) has released the following
Pulmicort Turbuhaler (budesonide inhalation powder) 200 mcg 60 Metered Doses
For Oral Inhalation, Rx Only, Professional Sample. Recall # D-349-2.
CK1524, CK1527, CK1539, CK1547- Exp. Date Apr-03
CL1555, CL1560, CL1562, CL1564, CL1566-Exp. Date May-03 CM1589- Exp. Date
Recalling Firm: Astrazeneca, Wilmington, DE, by letter on June 10, 2002.
Manufacturer: Astrazeneca Liquid Production, Sodertalje, Sweden
Firm initiated recall is ongoing.
The turbuhaler may deliver a super-potent dose.
VOLUME OF PRODUCT IN COMMERCE