IntelliVue G7m Anesthesia Gas Module — Class II medical device recall Z-2689-2020
Ongoing recall by Philips North America, LLC, reported 2020-07-29, distributed nationwide. The device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and
| Recall number | Z-2689-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, LLC, Andover, MA, United States |
| Recall initiated | 2020-06-25 |
| Classified | 2020-07-23 |
| Reported by FDA | 2020-07-29 |
| Distributed | Nationwide (US) |
| Quantity | 3,075 |
| Reason classes | software |
| Serial numbers | DE4, DE43803614, DE43803616, DE43803617, DE43803618, DE43803620, DE43803621, DE43803647, DE43803648, DE43803649, DE43803650, DE43803651, DE43803652, DE43803653, DE43803654, DE43803655, DE43803656, DE43803657, DE43803658, DE43803659, DE43803660, DE43803661, DE43803662, DE43803663, DE43803664 and 475 more |
| Model numbers | 866173 |
Product
IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391, 453564477401, 866173
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2689-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.