Philips Digital Diagnost with patient carriage Model: 712050 with… — Class II medical device recall Z-2494-2012
Terminated recall by Philips Healthcare Inc., reported 2012-10-10, distributed nationwide. Hook does not securely hold the footplate in vertical position, causing the footplate to disengage and may fal
| Recall number | Z-2494-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2012-09-12 |
| Classified | 2012-09-28 |
| Reported by FDA | 2012-10-10 |
| Terminated | 2013-07-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BH, CA, CH, CL, CN, CZ, DE, DK, ES, FI, FR, GB, IE, IT, JP, KR, NL, NO, NZ, PL, QA, RO, RU, SA, SE, SK, TH, TR, TW, ZA |
| Quantity | 536 units |
| Model numbers | 712050 |
Product
Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543. Product Usage: Stationary radiographic System
Reason for recall
Hook does not securely hold the footplate in vertical position, causing the footplate to disengage and may fall on patient or operator
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-2494-2012. 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.