Class II

Medical Device Recall: GYN LAPAROSCOPY PACK. Medical convenience kit.

AVID Medical, Inc. · June 11, 2025

Reason for Recall

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Distribution

Domestic: CA, IL, MD, OH, PA, TX, WA.

States Affected

CA, IL, MD, OH, PA, TX, WA

Quantity Affected

346 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2250-2025

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.