DigitalDiagnost C50 — Class II medical device recall Z-2498-2019
Terminated recall by Philips Healthcare, reported 2019-10-02, distributed in PR. During recent evaluations of the Philips DigitalDiagnost C50 system, Philips identified a missing label. This
| Recall number | Z-2498-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Philips Healthcare, Andover, MA, United States |
| Recall initiated | 2018-12-21 |
| Classified | 2019-09-20 |
| Reported by FDA | 2019-10-02 |
| Terminated | 2020-10-27 |
| Distributed | PR |
| Quantity | 2 |
| Reason classes | labeling |
| Serial numbers | SN170053, SN180074 |
Product
DigitalDiagnost C50, Stationary X-ray System
Reason for recall
During recent evaluations of the Philips DigitalDiagnost C50 system, Philips identified a missing label. This notification is intended to provide you with information regarding what the issue is, and relevant affected product, the actions you are required to take and the actions planned by Philips to correct the issue. If you need any or further information or support concerning this issue, please contact your local Philips representative or Philips Customer Service: 1-800-722-9377.
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-2498-2019. 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.