Nipro Medical Corporation: Medical Device Recall in 2018 - (Recall #: Z-1876-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24 lines per case. The Nipro¿ Set - Blood Tubing Set with Transducer Protector and Priming Set are disposable bloodlines intended to provide extracorporeal access to the patient s blood during hemodialysis. The compatibility of available configurations is the responsibility of the physician in charge.

Product Classification:

Class II

Date Initiated: December 19, 2017

Date Posted: May 23, 2018

Recall Number: Z-1876-2018

Event ID: 79834

Reason for Recall:

There is a possibility of the heparin line is occluded.

Status: Terminated

Product Quantity: 307,944 units.

Code Information:

Model No. BL+A223D/V809D, Vendor Batch No. 17I06-9, 17I16-9, 17I18-9, 17J17-9, 17J19-9 , 17J20-9 , 17J21-9, 17I19-9, 17K07-9 , 17I01-9, 17J12-9, 17J16-9, 17I21-9, 17I25-9, 17I26-9, 17J09-9, 17J11-9, 17K15-9, 17K16-9.

Distribution Pattern:

US Distribution to the states of : GA, NY, TN, TX.

Voluntary or Mandated:

Voluntary: Firm initiated