FDA Device recall Z-1062-2017
Velara Generator with an old Firmware version used with the Philips Integris BH5000
- FDA Device
- Class II
- terminated
- Published 2017-02-01
On 2017-02-01 the FDA classified a Class II recall of Velara Generator with an old Firmware version used with the Philips Integris BH5000 by Philips Electronics North America, citing system may lock up.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1062-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-12-09 |
| Published | 2017-02-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Electronics North America |
| Distribution | AL, CA, DC, GA, IL, KS, MD, MO, NC, NY, OH, PA, RI, SC, TX, WA |
Product
Velara Generator with an old Firmware version used with the Philips Integris BH5000
Reason
System may lock up.
Identifiers
| code_info | Velara Generator with 12nc number: 989000070011, 989000070122, 989000070123, 989000070124, 989000070125, 989000070126, 989000070321 |
|---|
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-1062-2017%22
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