FDA Enforcement Class I Ongoing

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

Recall: Z-1002-2026 · Reported January 14, 2026

Enforcement

Recall Number
Z-1002-2026
Event ID
98060
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
AVID Medical, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
January 14, 2026
Initiation Date
November 11, 2025
Classification Date
January 2, 2026
Address
9000 Westmont Dr, Toano, VA, 23168-9351, United States

Description

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

Reason

Devices are not suitable for organ transplant.

Code Info

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

Distribution

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

Quantity

380 units