Philips Diagnost Stationary Radiographic System Models: 712020 — Class II medical device recall Z-1447-2013
Terminated recall by Philips Healthcare Inc., reported 2013-06-26, distributed nationwide. Installation Acceptance Test Document (IATD) non compliant with regulations IATDs (Installation Acceptance Tes
| Recall number | Z-1447-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2013-01-16 |
| Classified | 2013-06-17 |
| Reported by FDA | 2013-06-26 |
| Terminated | 2016-09-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 177 units |
| Serial numbers | 248244, 304009, 316236, 325939, 325940, 340184, 347726, 348997, 351083, 351896, 353318, 354256, 355621, 355644, 355646, 355648, 356131, 356153, 356334, 356526, 356983, 357275, 357413, 357888, 358322 and 150 more |
| Model numbers | 712020, 712022, 712050, 712052, 712055, 712057, 712062 |
Product
Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product Usage: Universal RAD Applications
Reason for recall
Installation Acceptance Test Document (IATD) non compliant with regulations IATDs (Installation Acceptance Test could not be located or different templates have been used
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-1447-2013. 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.