Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost — Class II medical device recall Z-2465-2012
Terminated recall by Philips Healthcare Inc., reported 2012-10-03, distributed nationwide. The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile Detector Holder and may fall down
| Recall number | Z-2465-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2012-09-06 |
| Classified | 2012-09-27 |
| Reported by FDA | 2012-10-03 |
| Terminated | 2017-01-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CA, CH, CL, DE, FI, FR, GB, HU, IT, JP, KR, LV, NL, NZ, OM |
| Quantity | 93 units |
| Serial numbers | SN10000018, SN10000038, SN10000053, SN10000101, SN10000102, SN10000107, SN10000113, SN10000246, SN10000297, SN10000363, SN10000407, SN10000413, SN10000414, SN10000416, SN10000424, SN10000442, SN10000468, SN10000482, SN10000512, SN10000515, SN10000537, SN10000544, SN10000554, SN10000557, SN10000635 and 68 more |
Product
Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single Detector, Dual Detector, Release 3) System codes: 712020, 712022, 712025 This system is used for making X-ray exposures for diagnostics.
Reason for recall
The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile Detector Holder and may fall down
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-2465-2012. 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.