← FDA ENFORCEMENT
Z-1688-2026Class II
Stryker Communications
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
Stryker Communications
Product type
Device
Status
Ongoing
Report date
2026-04-08
Distribution
Worldwide - US Nationwide distribution.
Firm state
TX
Product quantity
6170 units
Initiated by
Voluntary: Firm initiated
Reason for recall
Surgical light assembly may not adequate support the weight of the ceiling cover.
Product description
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Code / lot info
UDI: 07613327296167; All Lots
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →