RecallRadar

FDA Device recall Z-0661-2014

183 cm (72") Smallbore Quadfuse Ext Set w/4 NanoClave¿ (Yellow, Green Rings), 4 Anti-Syphon Valves, 0.2 Micron Positive Filter, BCVClave ¿,…

On 2014-01-15 the FDA classified a Class II recall of 183 cm (72") Smallbore Quadfuse Ext Set w/4 NanoClave¿ (Yellow, Green Rings), 4 Anti-Syphon Valves, 0.2 Micron Positive Filter, BCVClave ¿,… by Icu Medical, citing ICU Medical is recalling certain lots of the NanoClave Needlefree Connector product line because of a small percentage of devices that may leak.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0661-2014
ClassificationClass II
Statusterminated
Initiated2013-12-24
Published2014-01-15
Last updated2026-09-13 11:53 UTC
CompanyIcu Medical
DistributionAL, CA, GA, HI, IL, IN, KY, NC, NH, OH, TN, TX, UT, VT, WI

Product

183 cm (72") Smallbore Quadfuse Ext Set w/4 NanoClave¿ (Yellow, Green Rings), 4 Anti-Syphon Valves, 0.2 Micron Positive Filter, BCVClave ¿, NanoClave¿ T-Connector, Rotating Luer, Part No. A1000, Item No. 011-A1094 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intravascular administration set for the administration of fluids to a patient through a cannula placed in the vein or artery.

Reason

ICU Medical is recalling certain lots of the NanoClave Needlefree Connector product line because of a small percentage of devices that may leak.

Identifiers

code_infoItem No. 011-A1094. Lot No. 2776971, 2785649, 2796670.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0661-2014%22

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