Phillips Respironics, Inc.

FDA Regulatory Profile

Phillips Respironics, Inc. appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1143-2014, Class I) was initiated on February 11, 2014.

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1143-2014Class ITrilogy Ventilators The Respironics Trilogy 100 system provides continuous or intermittent ventilatFebruary 11, 2014