Chromophare Surgical Light System — Class II medical device recall Z-1506-2024
Ongoing recall by Stryker Communications, reported 2024-04-17. Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.
| Recall number | Z-1506-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Communications, Flower Mound, TX, United States |
| Recall initiated | 2024-02-08 |
| Classified | 2024-04-09 |
| Reported by FDA | 2024-04-17 |
| Quantity | 1 units |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 07613327296167 |
| Model numbers | CH00000001 |
Product
Chromophare Surgical Light System , REF CH00000001
Reason for recall
Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.
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-1506-2024. 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.