Facility

NOVO NORDISK A/S

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)	3003131673
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	BRENNUM PARK HILLEROED Hovedstaden, DK DK-3400
Registration status	Active · expires 2026
Parent company	NOVO NORDISK INC. (owner-operator 9027307)
Brand names	NovoTwist 30G; NovoTwist 32G Tip

Activity by year

Recalls (1)

Devices registered here (1)

Needle, Hypodermic, Single Lumen
Product code FMI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570

Recalls & enforcement

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

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 A/S (FEI 3003131673) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003131673-novo-nordisk-a-s/

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