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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 Recall of Tripedia(TM) VaccineOn January 27, 1999, the Food and Drug Administration initiated a voluntary recall of Tripedia(TM) diphtheria and tetanus toxoids and acellular pertussis vaccine (DTaP), lot number 0916490, manufactured by Pasteur Merieux Connaught USA. * Routine post-release stability testing completed in January 1999 indicated that the potency of the diphtheria toxoid component of this lot was below specification. The potency of the tetanus and pertussis components of this lot was acceptable. The lot was distributed during February-June 1998. All lots of Tripedia(TM) met potency specifications before release. Previously tested lots of Tripedia(TM) met diphtheria potency specifications in routine stability testing after release; stability testing of additional lots is in progress. A primary series (three doses) of fully potent diphtheria toxoid-containing vaccine is required to reliably induce protective antibody levels. Five doses of diphtheria toxoid-containing vaccine are recommended for preschool-aged children in the United States and provide optimal protection against diphtheria. The risk for exposure to toxigenic strains of Corynebacterium diphtheriae in the United States is low; however, diphtheria remains endemic in many countries. Additional doses of diphtheria toxoid-containing vaccine beyond those recommended in the childhood immunization schedule are associated with an increase in local reactions and should be considered only for children vaccinated with Tripedia(TM) lot number 0916490 who may be at increased risk for exposure to toxigenic strains of C. diphtheriae. CDC, the American Academy of Pediatrics, and the American Academy of Family Physicians have developed recommendations for children who received one or more doses of Tripedia(TM) lot number 0916490. The complete text of the recommendations is available on CDC's National Immunization Program World-Wide Web site, http://www.cdc.gov/nip/news/recall.htm; in summary, the recommendations are as follows:
* Use of trade names and commercial sources is for identification only and does not imply endorsement by CDC or the U.S. Department of Health and Human Services. ** Travelers may be at substantial risk for exposure to toxigenic strains of C. diphtheriae, especially with prolonged travel, extensive contact with children, or exposure to poor hygiene. Countries comprise the following: Africa -- Algeria, Egypt, and sub-Saharan Africa; Americas -- Brazil, Dominican Republic, Ecuador, and Haiti; Asia/Oceania -- Afghanistan, Bangladesh, Cambodia, China, India, Indonesia, Iran, Iraq, Laos, Mongolia, Myanmar, Nepal, Pakistan, Philippines, Syria, Thailand, Turkey, Vietnam, and Yemen; and Europe -- Albania and all countries of the former Soviet Union. Table_1 Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size. TABLE 1. Recommendations for children who travel to areas where the risk for diphtheria is high* and who received Tripedia(TM) diphtheria and tetanus toxoids and acellular pertussis vaccine (DTaP) lot number 0916490+ ======================================================================================================= Total doses received of any diphtheria No. doses of toxoid-containing Tripedia(TM) from lot Age (mos) vaccine no. 0916490 Recommendation& ----------------------------------------------------------------------------------------------- 2-11 1-2 1-2 Complete primary series with DTaP@ 3 1 Administer fourth dose of DTaP at age 15-18 mos 3 2-3 Administer supplemental dose of DT, followed by fourth dose of DTaP at age 15-18 mos ----------------------------------------------------------------------------------------------- >=12 3 1 Administer fourth dose of DTaP at age 15-18 mos 3 2-3 Administer supplemental dose of DT if <6 months have elapsed since third dose of DTaP, followed by fourth dose of DTaP at age 15-18 mos OR Administer fourth dose of DTaP as early as age 12 mos if >=6 months have elapsed since third dose of DTaP 4 1-3 Administer fifth dose of DTaP at age 4 to 6 yrs 5 1 Administer routine tetanus and diphtheria toxoids (for adolescent and adult use) boosters ----------------------------------------------------------------------------------------------- * Travelers may be at substantial risk for exposure to toxigenic strains of Corynebacterium diphtheriae, especially with prolonged travel, extensive contact with children, or exposure to poor hygiene conditions. Countries comprise the following: Africa--Algeria, Egypt, and sub-Saharan Africa; Americas--Brazil, Dominican Republic, Ecuador, and Haiti; Asia/Oceania-- Afghanistan, Bangladesh, Cambodia, China, India, Indonesia, Iran, Iraq, Laos, Mongolia, Myanmar, Nepal, Pakistan, Philippines, Syria, Thailand, Turkey, Vietnam, and Yemen; and Europe--Albania and all countries of the former Soviet Union. + Manufactured by Pasteur Mórieux Connaught USA. Use of trade names and commercial sources is for identification only and does not imply endorsement by CDC or the U.S. Depart- ment of Health and Human Services. & The minimum interval is 4 weeks between a dose of diphtheria and tetanus toxoids (for pediatric use) (DT) and any other dose of diphtheria toxoid-containing vaccine. The minimum interval is 6 months between the third dose of DTaP (including doses of Tripedia(TM) lot number 0916490) and the fourth dose of DTaP. @ If time is sufficient before travel, children who received two doses of Tripedia(TM) lot number 0916490 should receive their third dose of DTaP (as early as 4 weeks after the previous dose of DTaP) and a supplemental dose of DT (as early as 4 weeks after the third dose of DTaP). ======================================================================================================= Return to top. Disclaimer All MMWR HTML versions of articles are electronic conversions from ASCII text into HTML. This conversion may have resulted in character translation or format errors in the HTML version. Users should not rely on this HTML document, but are referred to the electronic PDF version and/or the original MMWR paper copy for the official text, figures, and tables. An original paper copy of this issue can be obtained from the Superintendent of Documents, U.S. Government Printing Office (GPO), Washington, DC 20402-9371; telephone: (202) 512-1800. Contact GPO for current prices. **Questions or messages regarding errors in formatting should be addressed to mmwrq@cdc.gov.Page converted: 02/25/99 |
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