FDA Device recall Z-1488-2020
Integris Allura 9, system codes 722018 722021
- FDA Device
- Class II
- terminated
- Published 2020-03-25
On 2020-03-25 the FDA classified a Class II recall of Integris Allura 9, system codes 722018 722021 by Philips North America, citing A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1488-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-30 |
| Published | 2020-03-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Integris Allura 9, system codes 722018 722021
Reason
A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.
Identifiers
| code_info | Serial Codes 8 114 64 906187 41 38 119 75 25 87 67 107 32 97 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1488-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.