Trilogy 100 — Class II medical device recall Z-1065-2016
Terminated recall by Philips Respironics, reported 2016-03-16, distributed nationwide. Software Issue
| Recall number | Z-1065-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Respironics, Monroeville, PA, United States |
| Recall initiated | 2016-01-18 |
| Classified | 2016-03-07 |
| Reported by FDA | 2016-03-16 |
| Terminated | 2017-05-26 |
| Distributed | Nationwide (US) |
| Quantity | 104,508 units |
| Reason classes | software |
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.
Reason for recall
Software Issue
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.