FDA Device recall Z-2669-2016
Allura Xper with release R8.2: Allura Xper FD10, 722026
- FDA Device
- Class II
- terminated
- Published 2016-09-07
On 2016-09-07 the FDA classified a Class II recall of Allura Xper with release R8.2: Allura Xper FD10, 722026 by Philips Electronics North America, citing increase in the failure rate of certain low-voltage DC power supplies ( DCPS ).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2669-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-07 |
| Published | 2016-09-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Electronics North America |
| Distribution | US |
Product
Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper FD20, 722028; Allura Xper FD20/10 biplane, 722029; Allura Xper FD10 OR Table, 722033; Allura Xper FD10/10 OR Table, 722034; Allura Xper FD20 OR Table, 722035; Allure Xper FD20/20 , 722038; Allura Xper FD20/20 biplane OR Table, 722039; Allura Xper FD20/15, 722058; Allura Xper FD20/15 OR Table, 722059
Reason
Increase in the failure rate of certain low-voltage DC power supplies ( DCPS )
Identifiers
| code_info | Allura Xper with release R8.2, |
|---|
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-2669-2016%22
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