Drug recall
Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
FDA recall event 97285 · Class II · Stryker Communications
Key facts
| Event ID | 97285 |
|---|---|
| Recall numbers | Z-2620-2025 |
| Recalling firm | Stryker Communications |
| Product type | Devices |
| Products | Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur. |
| Initiation date | Jul 15, 2025 |
| Report date | Oct 1, 2025 |
| City | Flower Mound |
| State | TX |
| Country | United States |
| FEI number | 3002975342 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: