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Respironics, Inc. Completes Voluntary Recall Notification of a Limited Number of Trilogy 100 Ventilators

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 Adverse reactions and/or quality problems should also be reported to Respironics at 1-877-387-3311. 

Serial Numbers of Domestic Devices RecalledTV111021835








































SOURCE Respironics, Inc.
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