Philips Respironics, Inc.: Medical Device Recall in 2023 - (Recall #: Z-0884-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Philips Garbin Ventilator, Model Number 1058180B

Product Classification:

Class I

Date Initiated: December 7, 2022

Date Posted: January 18, 2023

Recall Number: Z-0884-2023

Event ID: 91293

Reason for Recall:

The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air inlet, which could result in a reduction in delivered therapy volume or pressure and could cause the device to alarm.

Status: Ongoing

Product Quantity: 9

Code Information:

UDI: 00606959429338; Serial Numbers: GV119100314 GV118011626 GV117030343 GV117020301 GV11910210D GV117060237 GV11807062D GV119070802 GV11605061E

Distribution Pattern:

US Nationwide and Global Distribution to countries of: Australia, Brazil, Canada, China, Germany, Japan, Korea, and Latin America.

Voluntary or Mandated:

Voluntary: Firm initiated