Class II

Medical Device Recall: Chromophare Surgical Light System , REF CH00000001

Stryker Communications · February 8, 2024

Reason for Recall

Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.

Distribution

US: None OUS: Chili

Quantity Affected

1 unit

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1506-2024

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.

Stryker Communications Medical Device Recall: Chromophare Surgical Light System , REF CH00000001 | SafeCheck