Philips Respironics Recalls

Overview of recall records associated with Philips Respironics, including dates, categories and classifications where available.

1recall records

Mar 16, 2016latest record date

Mar 16, 2016earliest record date

Recall history in this database

Classification mix: Class II: 1.

Medical DeviceMar 16, 2016

Philips Respironics Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin recall — FDA Z-1065-2016

Software Issue

Class IIFDA: TerminatedPhilips Respironics

Understanding this recall history

This page summarizes recall records in which the official source identifies Philips Respironics as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.