Vue Motion V12 — Class II medical device recall Z-1692-2026
Ongoing recall by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., reported 2026-04-08, distributed nationwide. Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display ou
| Recall number | Z-1692-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best, Netherlands |
| Recall initiated | 2026-03-05 |
| Classified | 2026-03-27 |
| Reported by FDA | 2026-04-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BE, BO, BR, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GR, HN, HU, ID, IE, IL, IN, IS, IT, JO, JP, KW, LB, MA, MX, MY, NL, NO, NZ, OM, PA, PE, PH, PL, PT, QA, RO, RS, SA, SE, SG, SI, SK, TH, UY, VN, ZA |
| Quantity | 3,552 units |
| UPC / GTIN / UDI-DI | 00884838100336, 00884838100343, 00884838100350, 00884838100367 |
Product
Vue Motion V12. Product Number: 1017979.
Reason for recall
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
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-1692-2026. 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.