Z-2289-2021 Class II Ongoing

Recalled by Philips Respironics, Inc. — Murrysville, PA

Recall Details

Product Type
Devices
Report Date
August 25, 2021
Initiation Date
July 26, 2021
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
18936 (US); 4659 (OUS)

Product Description

Trilogy EV300, Product numbers CA2200X12B, DS2200X11B, FX2200X15B, IN2200X15B

Reason for Recall

Two software issues have been identified related to pressure increase in the device: The first issue is described as "Infant/Pediatric EFS Calibration Pressure Increase" and the second issue is described as "Pressure Drift (Continuous Usage).

Distribution Pattern

Worldwide distribution - US nationwide distribution.

Code Information

Software version numbers 1.02.01.00, 1.03.05.00, 1.03.07.00, 1.04.02.00, 1.04.06, 1.05.01, and 1.06.02