Philips Healthcare TraumaDiagnost — Class II medical device recall Z-0766-2016
Terminated recall by Philips Electronics North America Corporation, reported 2016-02-17, distributed in AL, CA, FL, GA, KS, MA, NY, RI…. If arm is not fastened securely it could fall down.
| Recall number | Z-0766-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Electronics North America Corporation, Andover, MA, United States |
| Recall initiated | 2015-07-22 |
| Classified | 2016-02-05 |
| Reported by FDA | 2016-02-17 |
| Terminated | 2020-10-14 |
| Distributed | AL, CA, FL, GA, KS, MA, NY, RI, TX, WI |
| Countries outside the US | AT, AU, BE, CA, CH, DE, ES, FR, IE, IT, NL, NZ, PT, ZA |
Product
Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.
Reason for recall
If arm is not fastened securely it could 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-0766-2016. 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.