AVID Medical, Inc.: Device Recall

Recall #Z-2248-2025 · 06/11/2025

Class II: Risk

Recall Details

Recall Number
Z-2248-2025
Classification
Class II
Product Type
Device
Recalling Firm
AVID Medical, Inc.
Status
Ongoing
Date Initiated
06/11/2025
Location
Toano, VA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
203 units

Reason for Recall

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

Product Description

GENERAL ROBOTIC PACK. Medical convenience kit.

Distribution Pattern

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

Other Recalls by AVID Medical, Inc.

View all recalls by AVID Medical, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.