Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
- Recalling company
- Stryker Communications
- Product
- Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
- Reason
- Surgical light assembly may not adequate support the weight of the ceiling cover.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 23, 2026
- Reported
- Apr 8, 2026
- Distribution
- Worldwide - US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 6170 units
- Lot / codes
- UDI: 07613327296167; All Lots
- Company location
- Flower Mound, TX
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1688-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1688-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.