FDA Device recall Z-1787-2012
GE Healthcare, Aestiva/5 7900 SmartVent, anesthesia machine
- FDA Device
- Class I
- terminated
- Published 2012-06-27
On 2012-06-27 the FDA classified a Class I recall of GE Healthcare, Aestiva/5 7900 SmartVent, anesthesia machine by Ge Healthcare, citing GE Healthcare has recently become aware of a potential safety issue due to the interlock slide mechanism missing from the 3-vaporizer manifold of your Aestiva 7900 Anesthesia Devi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1787-2012 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-04-10 |
| Published | 2012-06-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Healthcare, Aestiva/5 7900 SmartVent, anesthesia machine. Used in Datex-Ohmeda Aestiva/5 Anesthesia Systems.
Reason
GE Healthcare has recently become aware of a potential safety issue due to the interlock slide mechanism missing from the 3-vaporizer manifold of your Aestiva 7900 Anesthesia Device. This Potential for two (2) vaporizers delivering agent at the same time. This could manifest as over delivery of a single agent if both vaporizers contain the same agent or as delivery of more than one agent. This m
Identifiers
| code_info | Serial Number AMRP01031 AMRP00966 AMRP01030 AMRP00968 AMRP00967 AMRP01033 AMRP00970 AMRP00969 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1787-2012%22
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