Patient Information Center iX and Patient Information Center iX Expand — Class II medical device recall Z-1827-2024
Ongoing recall by Philips North America Llc, reported 2024-05-22, distributed nationwide. Event Catalog information does not save when copied and transferred from one unit to another.
| Recall number | Z-1827-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America Llc, Cambridge, MA, United States |
| Recall initiated | 2024-04-19 |
| Classified | 2024-05-15 |
| Reported by FDA | 2024-05-22 |
| Distributed | Nationwide (US) |
| Serial numbers | 002A-5MGJ-6, 003W-3UN7-M, 0128-2WG5-0, 016X-52P8-4, 017L-0VKT-B, 032M-79HL-V, 041V-48PE-D, 064C-44NB-H, 067L-7MPL-2, 094B-40KU-3, 0A3U-6ZJ1-5, 0A61-74NU-C, 0B5K-10GT-X, 0C0L-0FKE-4, 0C5Y-7FHX-V, 0D1V-48PE-J, 0D6E-39G4-P, 0F6V-6XMZ-5, 0J71-6UGD-Z, 0K6E-39G4-5, 0M6B-7VM6-F, 0N1E-7HJU-5, 0P4Y-78J7-V, 0P5D-5VMH-V, 0R1W-2MNL-2 and 216 more |
| Model numbers | 866389, 866390 |
Product
Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.
Reason for recall
Event Catalog information does not save when copied and transferred from one unit to another.
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-1827-2024. 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.