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Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

Class II
Recalling firm
Stryker Communications
Reason for recall
Surgical light assembly may not adequate support the weight of the ceiling cover.
Affected products (lot / model / serial)
UDI: 07613327296167; All Lots
Units affected
6170 units
Distribution pattern
Worldwide - US Nationwide distribution.
Firm location
Flower Mound, TX, United States
Recall type
Voluntary: Firm initiated
Product type
Devices
Status
Ongoing
Recall number
Z-1688-2026
Recall initiated
February 23, 2026
FDA classification date
March 27, 2026
FDA report date
April 8, 2026
FDA event ID
98514
Last updated on HTM Vibe
July 24, 2026
View on openFDA