Z-0161-2016 Class II Terminated

Recalled by Nipro Medical Corporation — Miami, FL

Recall Details

Product Type
Devices
Report Date
November 4, 2015
Initiation Date
August 13, 2015
Termination Date
October 13, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
50,000 pieces

Product Description

Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring an extracorporeal circuit of larger volumes of blood.

Reason for Recall

Some 1 1/4" needles were packaged and labeled in the 1" blister package.

Distribution Pattern

Indiana

Code Information

Lot # 15C03