← FDA ENFORCEMENT
Z-1688-2026Class II

Stryker Communications

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 openFDA enforcement API. 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.