Z-1475-2015 Class II Terminated
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