FDA Enforcement Class II Terminated

216 cm (85") PVC/PUR Smallbore Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, MicroClave Clear, Clamp, Rotating Luer.

Recall: Z-2801-2018 · Reported August 22, 2018

Enforcement

Recall Number
Z-2801-2018
Event ID
80460
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
ICU Medical de Mexico, S.A. de C.V.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 22, 2018
Initiation Date
March 1, 2018
Classification Date
August 16, 2018
Termination Date
January 26, 2024
Address
Avenida Cuarzo 250, Ensenada, Ejido Maneadero, N/A, Mexico

Description

216 cm (85") PVC/PUR Smallbore Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, MicroClave Clear, Clamp, Rotating Luer.

Reason

ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.

Code Info

Item Number 011-AM3010. Lot Number 3424312, UDI Number (01) 1 0840619 09487 1 (17) 220301 (30) 50 (10) 3424312, Expiration Date 03/01/2022

Distribution

US distribution to AZ, MA, NC, OH, TX, VA, WA. Worldwide distribution to Belgium, France, Germany.

Quantity

50 pouches