Data Foundry

Medical device recalls 2024

Patient Information Center iX — Class II medical device recall Z-1386-2024

Ongoing recall by Philips North America, reported 2024-04-03, distributed nationwide. It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom rington

Recall numberZ-1386-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmPhilips North America, Cambridge, MA, United States
Recall initiated2024-02-28
Classified2024-03-27
Reported by FDA2024-04-03
DistributedNationwide (US)
Quantity257,183 units
UPC / GTIN / UDI-DI00884838104594, 00884838112070, 00884838121782
Serial numbers002A-5MGJ-6, 003W-3UN7-M, 016X-52P8-4, 017L-0VKT-B, 032M-79HL-V, 041V-48PE-D, 067L-7MPL-2, 094B-40KU-3, 0A61-74NU-C, 0B5K-10GT-X, 0C5Y-7FHX-V, 0D1V-48PE-J, 0D6E-39G4-P, 0F6V-6XMZ-5, 0J71-6UGD-Z, 0K6E-39G4-5, 0N1E-7HJU-5, 0P4Y-78J7-V, 0P5D-5VMH-V, 0R1W-2MNL-2, 0T1M-18LJ-R, 0T41-35J4-A, 0U28-2WG5-M, 0V4G-0EG2-B, 0V7B-4EJH-A and 183 more
Model numbers866389, 866390

Product

Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X

Reason for recall

It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom ringtones when iOS device screens were locked with a passcode.

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-1386-2024. 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.