Class II

Medical Device Recall: Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

Stryker Communications · February 23, 2026

Reason for Recall

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

Distribution

Worldwide - US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

6170 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1688-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.