FDA Device recall Z-2697-2020
IntelliVue MX700 patient monitor, model no. 865241
- FDA Device
- Class II
- terminated
- Published 2020-07-29
On 2020-07-29 the FDA classified a Class II recall of IntelliVue MX700 patient monitor, model no. 865241 by Philips North America, citing some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2697-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-30 |
| Published | 2020-07-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips North America |
| Distribution | CA, HI, MA, NY, UT |
Product
IntelliVue MX700 patient monitor, model no. 865241
Reason
Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding instructions were not followed, and may also cause the monitor to stop operating or prevent it from being switched on.
Identifiers
| code_info | Serial numbers DE58562415 DE58562344 DE58562353 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2697-2020%22
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