FDA Medical devices recall ·
Stryker CHROMOPHARE Softlit Ring Surgical Light System recall
- Recall number
- Z-1688-2026
- Date
- (initiated February 23, 2026)
- Company / brand
- Stryker Communications
571 Silveron Blvd, Flower Mound, TX, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 6170 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Why was it recalled?
Surgical light assembly may not adequate support the weight of the ceiling cover.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI: 07613327296167; All Lots
Distribution
Worldwide - US Nationwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1688-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.