IntelliVue MX700 patient monitor — Class II medical device recall Z-2697-2020
Terminated recall by Philips North America, LLC, reported 2020-07-29, distributed in CA, HI, MA, NY, UT. Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power
| Recall number | Z-2697-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, LLC, Andover, MA, United States |
| Recall initiated | 2020-06-30 |
| Classified | 2020-07-23 |
| Reported by FDA | 2020-07-29 |
| Terminated | 2024-01-25 |
| Distributed | CA, HI, MA, NY, UT |
| Countries outside the US | CR, IE, LB, PL |
| Quantity | 28 |
| Serial numbers | DE58562344, DE58562353, DE58562415 |
| Model numbers | 865241 |
Product
IntelliVue MX700 patient monitor, model no. 865241
Reason for recall
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.
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-2697-2020. 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.