Recall Z-1592-2015— ICU Medical, Inc.

Class II · Terminated

Class II FDA medical device recall by ICU Medical, Inc., initiated 2015-04-20, terminated 2015-11-24. It names one FDA 510(k) clearance: K964435. Product: 108" (274 cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock, Non-DEHP Tubing, Item No. B33326. Reason: ICU Medical is recalling MicroClave T-Connectors because they have potential connection separation issues that could lead to leakage..

Recalling firm
ICU Medical, Inc.
Classification
Class II
Status
Terminated
Initiated
2015-04-20
Terminated
2015-11-24
Firm location
San Clemente, CA, United States

510(k) clearances named in this recall

1 on FDA's record

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

108" (274 cm) Transfer Set w/Check Valve, MicroClave T-Connector, Anti-Siphon Valve, Clamp, Luer Lock, Non-DEHP Tubing, Item No. B33326

Reason for recall

ICU Medical is recalling MicroClave T-Connectors because they have potential connection separation issues that could lead to leakage.

Data sourced from openFDA. This site is unofficial and independent of the FDA.