FDA Device recall Z-2689-2020
IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391, 453564477401, 866173
- FDA Device
- Class II
- ongoing
- Published 2020-07-29
On 2020-07-29 the FDA classified a Class II recall of IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391, 453564477401, 866173 by Philips North America, citing the device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and display of gas levels and generating one or more technical or INOP al….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2689-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-06-25 |
| Published | 2020-07-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips North America |
| Distribution | US |
Product
IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391, 453564477401, 866173
Reason
The device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and display of gas levels and generating one or more technical or INOP alarms.
Identifiers
| code_info | Serial numbers: DE43804813 DE43804952 DE43804945 DE43806034 DE43806054 DE43803806 DE43803822 DE43803824 DE4380…Serial numbers: DE43804813 DE43804952 DE43804945 DE43806034 DE43806054 DE43803806 DE43803822 DE43803824 DE43803907 DE43803911 DE43803915 DE43803983 DE43803986 DE43803988 DE43803989 DE43806224 DE43803973 DE43803895 DE43804009 DE43803778 DE43803752 DE43803762 DE43803766 DE43803772 DE43803773 DE43803774 DE43803790 DE43805609 DE43804358 DE43804391 DE43805722 DE43804085 DE43804093 DE43803753 DE43803754 DE43803769 DE43803823 DE43803831 DE43803836 DE43803841 DE43805272 DE43805280 DE43805291 DE43805295 DE43803802 DE43803812 DE43803814 DE43803815 DE43803826 DE43803828 DE43805705 DE43805709 DE43805713 DE43805717 DE43805720 DE43805725 DE43805735 DE43805744 DE43805515 DE43805516 DE43805522 DE43805526 DE43805574 DE43805715 DE43805734 DE43804627 DE43804634 DE43804636 DE43804560 DE43804563 DE43804566 DE43804567 DE43804576 DE43804090 DE43804102 DE43804017 DE43804200 DE43804204 DE43804216 DE43804880 DE43804133 DE43804138 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2689-2020%22
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