Nipro Medical recalls
Nipro Medical appears in 11 official U.S. recall notices indexed by RecallRadar, most recently on 2025-12-17.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 11 |
|---|---|
| Published | 2012-10-31 to 2025-12-17 |
| By agency | FDA Device (11) |
| By classification | Class II (10), Class III (1) |
| By status | terminated (10), ongoing (1) |
| Distribution named in notices | GA, IN, NJ, NY, TN, TX, US |
Recalls
- Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
FDA Device · Class II · 2025-12-17 · Nipro Medical
Reason: Screw may loosen or fallout of Hemodialysis system - Nipro Blood Tubing set with Priming Set and Transducer Protectors
FDA Device · Class II · 2018-05-23 · Nipro Medical
Reason: There is a possibility of the heparin line is occluded. - NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Transducer Protectors and Priming Set A disposable bloodline intended to provid…
FDA Device · Class II · 2016-01-20 · Nipro Medical
Reason: Blood foaming was found during evaluation of the product. - NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch
FDA Device · Class III · 2016-01-13 · Nipro Medical
Reason: Device has the potential to have torn wings. - Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments…
FDA Device · Class II · 2015-11-04 · Nipro Medical
Reason: Some 1 1/4" needles were packaged and labeled in the 1" blister package. - NIPRO Safe Touch Safety Scalp Vein Set
FDA Device · Class II · 2014-06-25 · Nipro Medical
Reason: 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. - AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Stiff
FDA Device · Class II · 2012-10-31 · Nipro Medical
Reason: 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. - AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Straight/ Regular
FDA Device · Class II · 2012-10-31 · Nipro Medical
Reason: 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. - AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Straight/ Stiff
FDA Device · Class II · 2012-10-31 · Nipro Medical
Reason: 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. - AquaLiner Hydrophilic Guidewire 0.035" X 180cm, Angle / Regular
FDA Device · Class II · 2012-10-31 · Nipro Medical
Reason: 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. - AquaLiner Hydrophilic Guidewire 0.035" X 260cm, Angle/ Regular
FDA Device · Class II · 2012-10-31 · Nipro Medical
Reason: 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.