Class II — Stryker Communications
| Recalling firm | STRYKER CORP. |
|---|---|
| Registered facility | View this company's 61 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Due to insufficient mounting force the stability of surgical light system cannot be guaranteed. |
| Product | Chromophare Surgical Light System , REF CH00000001 |
| Quantity | 1 unit |
| Distribution | US: None OUS: Chili |
| Initiated | 2024-02-08 |
| Classified | 2024-04-09 |
| Recall number | Z-1506-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Stryker Communications (Z-1506-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94199/
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