Ingenia Ambition X — Class II medical device recall Z-0975-2024
Ongoing recall by Philips North America, reported 2024-02-14, distributed nationwide. Magnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MR
| Recall number | Z-0975-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, Cambridge, MA, United States |
| Recall initiated | 2022-01-06 |
| Classified | 2024-02-02 |
| Reported by FDA | 2024-02-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | DK, NO, SE |
| Quantity | 10 |
| UPC / GTIN / UDI-DI | 00884838090040 |
| Serial numbers | 100019, 100020, 100022, 100024, 100025, 100028, 100031, 100032, 100056, 100063, 47004, 47019, 47190, 47200, 47210, 47227, 47231, 47271, 47281 |
Product
Ingenia Ambition X (Product Number 781356) - HA FlexTrak II (Accessory Number 989710008732), patient transportation system
Reason for recall
Magnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MRI systems if the wheels are in the magnetic field.
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-0975-2024. 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.