17 cm — Class II medical device recall Z-0707-2014
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 number | Z-0707-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ICU Medical, Inc., San Clemente, CA, United States |
| Recall initiated | 2013-12-24 |
| Classified | 2014-01-09 |
| Reported by FDA | 2014-01-15 |
| Terminated | 2014-04-01 |
| Distributed | AL, CA, GA, HI, IL, KY, NC, NH, OH, TN, TX, UT, VT, WI |
| Quantity | 100 |
| Reason classes | packaging |
| Lot numbers | 2796668 |
| Model numbers | 011-A1096 |
Product
17 cm (7") Smallbore Trifuse Ext Set w/3 NanoClave¿ ( Light Blue, Lavender Rings), 3 Anti-Syphon Valves, Rotating Luer, Item #011-A1096, Lot # 2796668. 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-0707-2014. 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.