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Persons using assistive technology might not be able to fully access information in this file. For assistance, please send e-mail to: mmwrq@cdc.gov. Type 508 Accommodation and the title of the report in the subject line of e-mail. Notice to Readers: Manufacturer's Recall of Nasal Spray Contaminated with Burkholderia cepacia ComplexOn March 24, this notice was posted as an MMWR Dispatch on the MMWR website (http://www.cdc.gov/mmwr). CDC has been notified of a voluntary recall of over-the-counter oxymetazoline HCl 0.05% nasal spray because of intrinsic contamination with Burkholderia cepacia complex. The nasal spray is distributed as "Major Twice-A-Day 12 Hour Nasal Spray." The manufacturer (Propharma Inc., Miami, Florida) has recalled lot no. K4496, released in November 2003, with an expiration date of October 2006. Preliminary molecular epidemiology indicates that isolates related to the strain found in the nasal spray have
been recovered from patients in multiple states. Clinicians should be aware that patients using product from this lot number
might have been exposed to B. cepacia complex. Patients with underlying lung disease (especially cystic fibrosis) might be at increased risk for severe infections with B.
cepacia complex. Cases of B. cepacia complex infection or colonization associated with use of
this product should be reported to the local or state health department and CDC, telephone 800-893-0485.
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This page last reviewed 3/25/2004
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