AVID Medical, Inc.: Medical Device Recall in 2025 - (Recall #: Z-2248-2025)

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:

GENERAL ROBOTIC PACK. Medical convenience kit.

Product Classification:

Class II

Date Initiated: June 11, 2025

Date Posted: August 13, 2025

Recall Number: Z-2248-2025

Event ID: 97149

Reason for Recall:

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

Status: Ongoing

Product Quantity: 203 units

Code Information:

Model No. NAFB082-04, NAMC473-01; UDI: 10809160395691, 10809160375037; Kit Lot No. 1568211, 1576237, 1599515, 1599516, 1605944, 1613558, 1616420, 1613626, 1625831, 1627259, 1628672, 1632042, 1635911.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated