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 lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur. |
| Product | Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034 |
| Quantity | 40 |
| Distribution | US Nationwide distribution in the states of TX, IL, NY, UT, OR, AZ, VT, NY, IL, MN. |
| Initiated | 2025-07-15 |
| Classified | 2025-09-24 |
| Recall number | Z-2620-2025 |
| 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-2620-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97285/
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