AVID Medical, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0928-2026)

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:

Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.

Product Classification:

Class II

Date Initiated: November 14, 2025

Date Posted: December 24, 2025

Recall Number: Z-0928-2026

Event ID: 98045

Reason for Recall:

Potential for incomplete seal on header bag.

Status: Ongoing

Product Quantity: 300 units

Code Information:

Catalog Number: EUHM009-01. UDI-DI: 10809160346839. Lot Number: 1635477. Expiration Date: 5/29/2028.

Distribution Pattern:

US distribution to GA, IL, NE, MD.

Voluntary or Mandated:

Voluntary: Firm initiated