FDA Device recall Z-2939-2026
Lago X
- FDA Device
- Class II
- ongoing
- Published 2026-08-26
On 2026-08-26 the FDA classified a Class II recall of Lago X by Spectral Instruments, citing momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2939-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-07-24 |
| Published | 2026-08-26 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Spectral Instruments |
| Distribution | n/a |
Product
Lago X
Reason
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Identifiers
| code_info | All serial numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2939-2026%22
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