Philips Respironics recalls Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin,

Recalled March 16, 2016 · FDA recall Z-1065-2016 · Philips Respironics

Hazard

Software Issue · FDA Class II

Units

104,508 units

Sold at

Nationwide Distribution including Puerto Rico and Internationally to the US Virgin Islands.

Description

Software Issue

Product

Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation.

Manufacturer(s)

Philips Respironics

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →