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Respironics, Inc. Completes Voluntary Recall Notification of a Limited Number of Trilogy 100 Ventilators
Date:1/12/2012

Respironics notified the U.S. Food & Drug Administration (FDA) of its decision to voluntarily recall the affected product on October 7, 2011. Any adverse reactions experienced with the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch. Adverse reactions and/or quality problems should also be reported to Respironics at 1-877-387-3311. 

Serial Numbers of Domestic Devices RecalledTV111021835

TV111031420

TV111032905

TV111032935TV111022832

TV111031462

TV111032906

TV111032938TV111030853

TV111031554

TV111032909

TV111032939TV111030932

TV111032809

TV111032912

TV111032940TV111030947

TV111032811

TV111032913

TV111033001TV111030976

TV111032812

TV111032914

TV111033004TV111030978

TV111032822

TV111032920

TV111033005TV111031001

TV111032827

TV111032923

TV111033006TV111031011

TV111032829

TV111032924

TV111033009TV111031037

TV111032830

TV111032925

TV111033010TV111031045

TV111032832

TV111032926

TV111033016TV111031403

TV111032833

TV111032929

TV111033018TV111031413

TV111032901

TV111032934

TV111033019 


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SOURCE Respironics, Inc.
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