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Nipro Medical Corporation recalls Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and f
Recalled November 4, 2015 · FDA recall Z-0161-2016 · Nipro Medical
Hazard
Some 1 1/4" needles were packaged and labeled in the 1" blister package. · FDA Class II
Units
50,000 pieces
Sold at
Indiana
Description
Some 1 1/4" needles were packaged and labeled in the 1" blister package.
Product
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.
Manufacturer(s)
Nipro Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →