Regulatory document
Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential…
FDA Safety Communications · Information · USA · Dec 22, 2022
Key facts
| Title | Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PE-PUR Foam Debris: FDA Safety Communication |
|---|---|
| Issuer | FDA Safety Communications |
| Source | FDA Safety Communications |
| Document type | Information |
| Country or region | USA |
| Date | Dec 22, 2022 |
| Document | fda.gov |
| Issuer website | fda.gov |
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