Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 — Class II medical device recall Z-1688-2026
Ongoing recall by Stryker Communications, reported 2026-04-08, distributed nationwide. Surgical light assembly may not adequate support the weight of the ceiling cover.
| Recall number | Z-1688-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Communications, Flower Mound, TX, United States |
| Recall initiated | 2026-02-23 |
| Classified | 2026-03-27 |
| Reported by FDA | 2026-04-08 |
| Distributed | Nationwide (US) |
| Quantity | 6,170 units |
| UPC / GTIN / UDI-DI | 07613327296167 |
| Model numbers | CH00000001 |
Product
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Reason for recall
Surgical light assembly may not adequate support the weight of the ceiling cover.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1688-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.