Omnidiagnost Classic — Class II medical device recall Z-1054-2019
Terminated recall by Philips North America, LLC, reported 2019-04-03, distributed nationwide. The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement tha
| Recall number | Z-1054-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, LLC, Andover, MA, United States |
| Recall initiated | 2019-02-28 |
| Classified | 2019-03-23 |
| Reported by FDA | 2019-04-03 |
| Terminated | 2020-08-03 |
| Distributed | Nationwide (US) |
| Quantity | 1,696 |
| UPC / GTIN / UDI-DI | 00708023018193 |
| Serial numbers | 096B, 101, 102, 103, 104, 106, 107, 108, 109, 110, 111, 112, 113, 115, 11591, 116, 117, 118, 119, 120, 121, 122, 123, 1232, 124 and 198 more |
Product
Omnidiagnost Classic, Product Codes 70859, 708023, 708024, 708025 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray system with remote-controlled facilities. It performs a wide range of routine examinations and interventional procedures include: Gastro-intestinal examination Urography Bronchography Arthrography Hysterography Myelography Lymphography Skeletal radiography Tomography Venography/phlebography Special procedures that require subtracted and non-subtracted digital imaginginclude: Angiography Peripheral angiography (bolus chasing) Vascular and non-vascular interventional procedures.
Reason for recall
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
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-1054-2019. 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.