(1) Patient Information Center iX, Model No. 866389 (2) Patient… — Class II medical device recall Z-0731-2024
Ongoing recall by Philips North America, reported 2024-01-24, distributed nationwide. Push notifications may fail to send to the user under certain conditions. This could potentially result in pat
| Recall number | Z-0731-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, Cambridge, MA, United States |
| Recall initiated | 2023-11-28 |
| Classified | 2024-01-13 |
| Reported by FDA | 2024-01-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, BR, CA, CH, CZ, DE, DK, EE, ES, FI, FR, GB, ID, IE, IN, IT, JP, KR, LT, LU, MX, NL, NO, NZ, OM, PH, PL, RO, SA, SE, SG, SK, TH, ZA |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00884838104594, 00884838112070, 00884838121782 |
| Model numbers | 866389, 866390, 866424 |
Product
(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model No. 866390 (3) PIC iX Hardware, Model No. 866424
Reason for recall
Push notifications may fail to send to the user under certain conditions. This could potentially result in patient harm due to delay in detection of a change in patient condition.
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-0731-2024. 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.