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ICU Medical, Inc. recalls 28 cm (11") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer. Product Usage
Recalled July 19, 2017 · FDA recall Z-2719-2017 · ICU Medical
Hazard
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak. · FDA Class II
Units
6 units
Sold at
Distribution to Italy and France, and the following states in the US: AZ, OH, TX, WA.
Description
The connection between the Female Luer and the NanoClave¿ manifold has the potential for developing a leak.
Product
28 cm (11") 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).
Manufacturer(s)
ICU Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →