FDA Recall Terminated

ICU Medical, Inc. Cath Lab Kit W/3Port "ON" Manifold, Waste Bag, Syringe & TP4; Item Number: AG7843 Indicated for fluid flow directional control and for providing access port(s) for administration of solutions.

Recall: Z-2208-2008 · Initiated June 11, 2008

Recall

Recall Number
Z-2208-2008
Event Number
48681
Firm
ICU Medical, Inc.
FEI Number
2025816
Product Code
FMG
Status
Terminated
Root Cause
Process change control
Initiated
June 11, 2008
Posted
September 16, 2008
Terminated
April 13, 2010
Address
951 Calle, Amanecer San Clemente, CA, 92673-6212

Description

ICU Medical, Inc. Cath Lab Kit W/3Port "ON" Manifold, Waste Bag, Syringe & TP4; Item Number: AG7843 Indicated for fluid flow directional control and for providing access port(s) for administration of solutions.

Reason

Improper orientation of the stopcock handle questions whether there is an adequate gas path to assure sterility, which presents a possible compromise of sterility.

Action

Every customer both direct and distributors who have purchased the affected lots were mailed a Product Recall Letter with attached fax-back Product Inventory Summary attachment on 06/11/2008 via fax and followed by UPS overnight delivery. The Product Recall Letter informed the customers of the reason for the recall and instructed them to complete and return the attached Product Inventory Summary. Instructions were also given for returning product in their inventory to ICU.

Distribution

Nationwide Distribution

Quantity

100