Facility

NEILMED PHARMACEUTICALS, INC.

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3026238784
Establishment type	Manufacture Medical Device
Location	981 S WANAMAKER AVE. Ontario, CA, US 91761
Registration status	Active · expires 2026
Parent company	NEILMED PHARMACEUTICALS, INC. (owner-operator 9041036)
Brand names	Sinus Rinse; Nasopure Nasal Wash

Activity by year

Recalls (1)

Devices registered here (1)

Irrigator, Sinus
Product code KAR (opens in a new tab) · Class I · Ear, Nose, Throat · 21 CFR 874.4420

Recalls & enforcement

Class IIOngoing2024-12-28
Due to nasal spray stability failure for bioburden.

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. “NEILMED PHARMACEUTICALS, INC. (FEI 3026238784) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3026238784-neilmed-pharmaceuticals-inc/

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