Medical device recalls Moderate risk

Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

Recall date
February 23, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1688-2026
FDA classification
Class II
Brand / firm
Stryker Communications
Sold / distributed
Worldwide - US Nationwide distribution.

Why it was recalled

Surgical light assembly may not adequate support the weight of the ceiling cover.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

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