Nipro Medical Corporation recalls Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and…
- Recall date
- August 13, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0161-2016
- FDA classification
- Class II
- Brand / firm
- Nipro Medical Corporation
- Sold / distributed
- Indiana
Why it was recalled
Some 1 1/4" needles were packaged and labeled in the 1" blister package.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
Get recall alerts
Free email alert whenever Nipro Medical Corporation has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Nipro Medical Corporation