FDA Enforcement Class II Ongoing

PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.

Recall: Z-2260-2025 · Reported August 13, 2025

Enforcement

Recall Number
Z-2260-2025
Event ID
97149
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
AVID Medical, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
August 13, 2025
Initiation Date
June 11, 2025
Classification Date
August 4, 2025
Address
9000 Westmont Dr, N/A, Toano, VA, 23168-9351, United States

Description

PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.

Reason

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

Code Info

Model No. NIHB0035-07; UDI: 10809160404959; Kit Lot No. 1591938, 1622268, 1628944, 1632685.

Distribution

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

Quantity

46 units