AVID Medical, Inc.: Medical Device Recall in 2025 - (Recall #: Z-2260-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.

Product Classification:

Class II

Date Initiated: June 11, 2025

Date Posted: August 13, 2025

Recall Number: Z-2260-2025

Event ID: 97149

Reason for Recall:

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

Status: Ongoing

Product Quantity: 46 units

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated