FDA recall Z-1688-2026
Stryker Communications · Class II · device
Product
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Reason for recall
Surgical light assembly may not adequate support the weight of the ceiling cover.
Distribution
Worldwide - US Nationwide distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2026-02-23
- Report date
- 2026-04-08
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Flower Mound, TX, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1688-2026