AVID Medical, Inc.: Device Recall

Recall #Z-2252-2025 · 06/11/2025

Class II: Risk

Recall Details

Recall Number
Z-2252-2025
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
20 units

Reason for Recall

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

Product Description

HVI CARDIAC ROBOT 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.