Stryker Communications recalls Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
- Recall date
- July 15, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2620-2025
- FDA classification
- Class II
- Brand / firm
- Stryker Communications
- Sold / distributed
- US Nationwide distribution in the states of TX, IL, NY, UT, OR, AZ, VT, NY, IL, MN.
Why it was recalled
Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
Get recall alerts
Free email alert whenever Stryker Communications has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Stryker Communications