Z-1475-2015 Class II Terminated

Recalled by Churchill Medical Systems, Inc. — Dover, NH

FDA device recall Z-1475-2015 was initiated by Churchill Medical Systems, Inc. on January 15, 2015 and is designated Class II. Reason for recall: Potential for leaking caused by insufficient bond between needleless device and female luer. The recall status is terminated (terminated February 25, 2016). Affected quantity: 6850.

Recall Details

Product Type
Devices
Report Date
April 29, 2015
Initiation Date
January 15, 2015
Termination Date
February 25, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
6850

Product Description

7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 Accessory device used to administer medical fluids

Reason for Recall

Potential for leaking caused by insufficient bond between needleless device and female luer.

Distribution Pattern

Nationwide Distribution including TX, OH, NY, CA, UT, PA, MA, NY, VA, and IL.

Code Information

1311028 1311040 1311041 1407066 1407197 1408055 1409055D 1410048D 1410157D