FDA Device recall Z-0766-2016
Philips Healthcare TraumaDiagnost
- FDA Device
- Class II
- terminated
- Published 2016-02-17
On 2016-02-17 the FDA classified a Class II recall of Philips Healthcare TraumaDiagnost by Philips Electronics North America, citing if arm is not fastened securely it could fall down.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0766-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-22 |
| Published | 2016-02-17 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Electronics North America |
| Distribution | AL, CA, FL, GA, KS, MA, NY, RI, TX, WI |
Product
Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.
Reason
If arm is not fastened securely it could fall down.
Identifiers
| code_info | All TraumaDiagnost products that were delivered before the week of July 2, 2007. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0766-2016%22
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