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 | Surgical light assembly may not adequate support the weight of the ceiling cover. |
| Product | Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001 |
| Quantity | 6170 units |
| Distribution | Worldwide - US Nationwide distribution. |
| Initiated | 2026-02-23 |
| Classified | 2026-03-27 |
| Recall number | Z-1688-2026 |
| 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-1688-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98514/
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