Z-1478-2015 Class II Terminated

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

FDA device recall Z-1478-2015 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: 1650.

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
1650

Product Description

6" Trifurcated set with Bionectors, Product Code: BN-944 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

1310051 1312063