Nipro Medical Recalls
11 recalls on record · October 31, 2012 to December 17, 2025 · Medical Devices
Recalls by year
12
14
15
16
18
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 17, 2025Medical DevicesFDA
Nipro Medical Corporation recalls Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Hazard: Screw may loosen or fallout of Hemodialysis system
May 23, 2018Medical DevicesFDA
Nipro Medical Corporation recalls Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24 line
Hazard: There is a possibility of the heparin line is occluded.
January 20, 2016Medical DevicesFDA
Nipro Medical Corporation recalls NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Transducer Protectors and Priming Set A disposable blood
Hazard: Blood foaming was found during evaluation of the product.
January 13, 2016Medical DevicesFDA
Nipro Medical Corporation recalls NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch. Item code FS+173230BC.
Hazard: Device has the potential to have torn wings.
November 4, 2015Medical DevicesFDA
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
Hazard: Some 1 1/4" needles were packaged and labeled in the 1" blister package.
June 25, 2014Medical DevicesFDA
Nipro Medical Corporation recalls NIPRO Safe Touch Safety Scalp Vein Set
Hazard: There is a possibility of a crack in the CP luer connector. The position of the crack is at the connection site of the CP luer connector and the tubing. The crack could cause or contribute to leakage of fluids.
October 31, 2012Medical DevicesFDA
Nipro Medical Corporation recalls AquaLiner Hydrophilic Guidewire 0.035" X 180cm, Angle / Regular. AquaLiner Hydrophilic Guidewire is designed for use
Hazard: Nipro Medical Corporation, Miami, FL recalled their AquaLiner Hydrophilic Guidewire because the wires contain insufficient lubricity which causes them to get stuck in the housing and become nonfunctional.
October 31, 2012Medical DevicesFDA
Nipro Medical Corporation recalls AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Straight/ Stiff. AquaLiner Hydrophilic Guidewire is designed for use
Hazard: Nipro Medical Corporation, Miami, FL recalled their AquaLiner Hydrophilic Guidewire because the wires contain insufficient lubricity which causes them to get stuck in the housing and become nonfunctional.
October 31, 2012Medical DevicesFDA
Nipro Medical Corporation recalls AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Straight/ Regular. AquaLiner Hydrophilic Guidewire is designed for us
Hazard: Nipro Medical Corporation, Miami, FL recalled their AquaLiner Hydrophilic Guidewire because the wires contain insufficient lubricity which causes them to get stuck in the housing and become nonfunctional.
October 31, 2012Medical DevicesFDA
Nipro Medical Corporation recalls AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Stiff. AquaLiner Hydrophilic Guidewire is designed for use in
Hazard: Nipro Medical Corporation, Miami, FL recalled their AquaLiner Hydrophilic Guidewire because the wires contain insufficient lubricity which causes them to get stuck in the housing and become nonfunctional.
October 31, 2012Medical DevicesFDA
Nipro Medical Corporation recalls AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Regular. AquaLiner Hydrophilic Guidewire is designed for use i
Hazard: Nipro Medical Corporation, Miami, FL recalled their AquaLiner Hydrophilic Guidewire because the wires contain insufficient lubricity which causes them to get stuck in the housing and become nonfunctional.