HA FlexTrak II-Patient transport functionality to transport the… — Class II medical device recall Z-1950-2024
Ongoing recall by Philips North America Llc, reported 2024-06-12, distributed nationwide. Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a po
| Recall number | Z-1950-2024 |
|---|---|
| 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 | 2024-05-03 |
| Classified | 2024-06-04 |
| Reported by FDA | 2024-06-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BD, BE, BH, BR, CA, CH, CL, CN, CO, CZ, DE, DK, EE, ES, FI, FR, GB, HK, HN, ID, IE, IN, IT, JO, JP, KR, LT, MA, MX, NL, NO, OM, PE, PL, SA, SE, SG, TH, TW, ZA |
| Quantity | 590 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00884838099500 |
| Serial numbers | 100018, 100019, 100020, 100022, 100023, 100024, 100025, 100026, 100027, 100028, 100029, 100030, 100031, 100032, 100033, 100034, 100036, 100038, 100039, 100041, 100042, 100043, 100044, 100045, 100046 and 475 more |
Product
HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710008732
Reason for recall
Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
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-1950-2024. 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.