FDA Device recall Z-0857-2026
IntelliVue MP80
- FDA Device
- Class II
- ongoing
- Published 2025-12-10
On 2025-12-10 the FDA classified a Class II recall of IntelliVue MP80 by Philips North America, citing potential issue where the IntelliVue monitors did not alarm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0857-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-10-31 |
| Published | 2025-12-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
IntelliVue MP80. Product Number: M8008A.
Reason
Potential issue where the IntelliVue monitors did not alarm.
Identifiers
| code_info | Product Number: M8008A; UDI-DI: 00884838000216; All Serial No. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0857-2026%22
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