FDA Recall Terminated

High Pressure Stopcock (3-Way, Luer Lock, Off). Product Usage: For IV.

Recall: Z-2128-2012 · Initiated April 17, 2012

Recall

Recall Number
Z-2128-2012
Event Number
62538
Firm
ICU Medical, Inc.
FEI Number
2025816
Product Code
DQO
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
April 17, 2012
Posted
August 2, 2012
Terminated
August 23, 2012
Address
951 Calle, Amanecer San Clemente, CA, 92673-6212

Description

High Pressure Stopcock (3-Way, Luer Lock, Off). Product Usage: For IV.

Reason

The firm initiated the recall due to a molding defect in a high pressure stopcock where a small percentage of the side ports could become totally occluded.

Action

ICU Medical sent an Urgent Medical Device Recall letter dated April 2012 to all affected customers. The letter identified the recalled product, problem and actions to be taken. Customers were instructed to inspect inventory, destroy affected products according to hospital protocol, complete and return verification form and contact ICU Customer Service to order replacement products. The letter states that ICU Medical will credit customer for any product destroyed once the completed verification form is received. This recall should be carried out to the user level and passed on to all those who need to be aware within your organization or any other organization the device may have been transferred to. Should you have any questions or require assistance relating to this recall please contact ICU Customer Service Monday through Friday between the hours of 8:30 AM and 4:00 PM Pacific time: 866-829-9025 and select option 8, or e-mail the following address: [email protected]

Distribution

Nationwide distribution

Quantity

4625