FDA Enforcement Class II Terminated

18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

Recall: Z-2716-2017 · Reported July 19, 2017

Enforcement

Recall Number
Z-2716-2017
Event ID
77560
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
ICU Medical, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 19, 2017
Initiation Date
May 30, 2017
Classification Date
July 11, 2017
Termination Date
September 20, 2024
Address
951 Calle Amanecer, San Clemente, CA, 92673-6212, United States

Description

18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

Reason

The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.

Code Info

Lot No. 3172948, 3192947, 3224228, 3246765, 3260270. Item No. 011-AM6111

Distribution

Distribution to Italy and France, and the following states in the US: AZ, OH, TX, WA.

Quantity

304 units