Philips Easy Diagnost Classic-Stationary x-ray system Catalog… — Class II medical device recall Z-2208-2012
Terminated recall by Philips Healthcare Inc., reported 2012-08-22, distributed in IN, MA, MI, MO, NC, NY, PA, SC…. Inclination switch in the stand may have been mounted incorrectly, as a result, the switch could not stop the
| Recall number | Z-2208-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2012-07-11 |
| Classified | 2012-08-15 |
| Reported by FDA | 2012-08-22 |
| Terminated | 2017-01-23 |
| Distributed | IN, MA, MI, MO, NC, NY, PA, SC, WI |
| Countries outside the US | CA, NZ |
| Quantity | 12 units |
| Reason classes | software |
| Serial numbers | 200081, 200115, 200148, 300114, SN07000109, SN07000141, SN07000667, SN5000162, SN5000421 |
| Model numbers | 706030, 706031, 706032, 70642, 70643 |
Product
Philips Easy Diagnost Classic-Stationary x-ray system Catalog Numbers: 70642, 70643, 706030, 706031, 706032 Stationary x-ray system, Universal RF system for general use.
Reason for recall
Inclination switch in the stand may have been mounted incorrectly, as a result, the switch could not stop the tilting movement of the table base due tol hardware or software errors.
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-2208-2012. 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.