Data Foundry

Medical device recalls 2014

6" — Class II medical device recall Z-0666-2014

Terminated recall by ICU Medical, Inc., reported 2014-01-15, distributed in AL, CA, GA, HI, IL, KY, NC, NH…. ICU Medical is recalling certain lots of the NanoClave Needlefree Connector product line because of a small pe

Recall numberZ-0666-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmICU Medical, Inc., San Clemente, CA, United States
Recall initiated2013-12-24
Classified2014-01-09
Reported by FDA2014-01-15
Terminated2014-04-01
DistributedAL, CA, GA, HI, IL, KY, NC, NH, OH, TN, TX, UT, VT, WI
Quantity700 units
Reason classespackaging
Lot numbers2773810, 2777115, 2781555
Model numbersA1000, A1001

Product

6" (15 cm) Appx 0.26 ml, Smallbore Ext Set w/Clamp, NanoClave¿ TConnector, Rotating Luer, Part No. A1000, Item No. A1001 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 for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0666-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.