AVID Medical, Inc.: Medical Device Recall in 2026 - (Recall #: Z-1002-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08

Product Classification:

Class I

Date Initiated: November 11, 2025

Date Posted: January 14, 2026

Recall Number: Z-1002-2026

Event ID: 98060

Reason for Recall:

Devices are not suitable for organ transplant.

Status: Ongoing

Product Quantity: 380 units

Code Information:

Kit Code: JACK097-08; UDI : 10809160462829; Lot No: 1654185.

Distribution Pattern:

US Nationwide distribution in the states of FL, GA and Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated