NIPRO CORPORATION
7 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (7)
Devices registered here (1)
- Needle, Ophthalmic SuturingProduct code HNM (opens in a new tab) · Class I · Ophthalmic · 21 CFR 886.4350
Recalls & enforcement
- Class IIOngoing2025-10-27Screw may loosen or fallout of Hemodialysis system
- Class IITerminated2017-12-19There is a possibility of the heparin line is occluded.
- Class IITerminated2015-08-13Some 1 1/4" needles were packaged and labeled in the 1" blister package.
- Class IITerminated2015-03-30Blood foaming was found during evaluation of the product.
- Class IIITerminated2014-04-01Device has the potential to have torn wings.
- Class IITerminated2013-05-04There 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.
- Class IITerminated2012-07-27Nipro 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.
Related
- All facilities operated by NIPRO CORPORATION
- Nipro (Thailand) Corporation Limited (TH)
- NIPRO MEDICAL CORPORATION (FL)
- NIPRO CORPORATION ODATE FACTORY (JP)
- NIPRO MEDICAL INDUSTRIES LTD. (JP)
- SHIBUYA CORPORATION (JP)
- PT. Nipro Indonesia Jaya (ID)
- NIPRO (SHANGHAI) CO., LTD. (CN)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “NIPRO CORPORATION (FEI 3000247873) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3000247873-nipro-corporation/
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