Recall
FDAHealthJune 5, 2025

Merit Medical Systems, Inc. — Custom Tubing Kit: REF: K04-00417, K04-00963, K04-01029

⚠️ High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line. Use of the affected product may result in the trapped air being introduced into the patient.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 5, 2025

US Nationwide distribution in the states of OH, CA, SD, VA, AZ, MT, TX, MI, FL, TN, PA, NJ, MN, ND, IA, LA, UT, KY, IL, OK, ME, IN, NY, NM, SC, AL, ID, CT, WI, GA, MA, NC, AR, WA.

What's affected?

Product
Custom Tubing Kit: REF: K04-00417, K04-00963, K04-01029
Lot code
(Expiration):

Additional details

REF/UDI-DI/Lot(Expiration): K04-00417/00884450046630/I3114667(12/10/2027), I3147550(1/28/2028); K04-00963/00884450046760/H3117053(12/14/2027), H3138590(1/20/2028), H3154108(2/10/2028), H3154786(2/10/2028), H3162244(2/19/2028), H3166789(3/2/2028), H3173526(3/23/2028); K04-01029/00884450148938/H3117059(12/17/2027), H3154112(2/10/2028), H3159017(2/19/2028), H3166777(3/9/2028), H3181994(4/1/2028);

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 2779.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.