Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nipro Safe Touch TULIP Safety Fistula Needle Recalled by Nipro Medical Corporation Due to Some 1 1/4" needles were packaged and labeled...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Nipro Medical Corporation directly.
Affected Products
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.
Quantity: 50,000 pieces
Why Was This Recalled?
Some 1 1/4" needles were packaged and labeled in the 1" blister package.
Where Was This Sold?
Indiana
About Nipro Medical Corporation
Nipro Medical Corporation has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report