Philips Respironics: Medical Device Recall in 2016 - (Recall #: Z-1065-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: January 18, 2016

Date Posted: March 16, 2016

Recall Number: Z-1065-2016

Event ID: 73177

Reason for Recall:

Software Issue

Status: Terminated

Product Quantity: 104,508 units

Code Information:

11 digit S/N begginning with GV or TV; also TGY1D01463

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated