FDA Device recall Z-1506-2024
Chromophare Surgical Light System , REF CH00000001
- FDA Device
- Class II
- ongoing
- Published 2024-04-17
On 2024-04-17 the FDA classified a Class II recall of Chromophare Surgical Light System , REF CH00000001 by Stryker Communications, citing due to insufficient mounting force the stability of surgical light system cannot be guaranteed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1506-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-08 |
| Published | 2024-04-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Stryker Communications |
| Distribution | n/a |
Product
Chromophare Surgical Light System , REF CH00000001
Reason
Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.
Identifiers
| code_info | S/N:03857056/ UDI: 07613327296167 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1506-2024%22
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