Facility

Novo Nordisk (China) Pharmaceuticals, Co. Ltd.

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

Key facts

1recalls · worst Class II

1inspections · worst NAI

—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)	3005186124
Establishment type	Manufacture Medical Device
Location	99 Nanhai Road Tianjin, CN 30045
Registration status	Active · expires 2026
Parent company	NOVO NORDISK INC. (owner-operator 9027307)
Brand names	NovoPen Echo

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Syringe, Piston
Product code FMF (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5860

Recalls & enforcement

Class IITerminated2017-07-05
A small number of batches may crack or break if exposed to certain chemicals, like certain cleaning agents.

FDA inspections (1)

NAI2017-11-02
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

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. “Novo Nordisk (China) Pharmaceuticals, Co. Ltd. (FEI 3005186124) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3005186124-novo-nordisk-china-pharmaceuticals-co-lt/

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