Mobile Diagnostic X-Ray System with Digital Panel — Class II medical device recall Z-1706-2017
Terminated recall by Philips Healthcare Inc., reported 2017-04-12, distributed nationwide. When the operator moves an image to another view then the electronic marker might be placed at the wrong anato
| Recall number | Z-1706-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2012-11-28 |
| Classified | 2017-04-04 |
| Reported by FDA | 2017-04-12 |
| Terminated | 2018-05-31 |
| Distributed | Nationwide (US) |
| Quantity | 220 systems |
Product
Mobile Diagnostic X-Ray System with Digital Panel
Reason for recall
When the operator moves an image to another view then the electronic marker might be placed at the wrong anatomical position in the resulting image.
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-1706-2017. 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.