AVID Medical, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0927-2026)

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, EP LAB PK. Catalog Number: ESJH009-03.

Product Classification:

Class II

Date Initiated: November 14, 2025

Date Posted: December 24, 2025

Recall Number: Z-0927-2026

Event ID: 98045

Reason for Recall:

Potential for incomplete seal on header bag.

Status: Ongoing

Product Quantity: 240 units

Code Information:

Catalog Number: ESJH009-03. UDI-DI: 10809160427316. Lot Code: Lot Number: 1653112. Expiration Date: 5/28/2028.

Distribution Pattern:

US distribution to GA, IL, NE, MD.

Voluntary or Mandated:

Voluntary: Firm initiated