FDA Enforcement Class I Ongoing

Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.

Recall: Z-1971-2026 · Reported May 13, 2026

Enforcement

Recall Number
Z-1971-2026
Event ID
98686
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
AVID Medical, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
May 13, 2026
Initiation Date
March 13, 2026
Classification Date
May 1, 2026
Address
9000 Westmont Dr, Toano, VA, 23168-9351, United States

Description

Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.

Reason

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Code Info

Model Number: DRCC36. UDI-DI (Kit Lot Numbers): 10809160469088 (1659651).

Distribution

US distribution to FL, IL, MO, MS, NC, NE, TX.

Quantity

180 kits