FDA Device recall Z-1688-2026
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
- FDA Device
- Class II
- ongoing
- Published 2026-04-08
On 2026-04-08 the FDA classified a Class II recall of Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 by Stryker Communications, citing surgical light assembly may not adequate support the weight of the ceiling cover.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1688-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-23 |
| Published | 2026-04-08 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Stryker Communications |
| Distribution | US |
Product
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Reason
Surgical light assembly may not adequate support the weight of the ceiling cover.
Identifiers
| code_info | UDI: 07613327296167; All Lots |
|---|
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-1688-2026%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.