Facility

CODAN US Corporation

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

Key facts

2recalls · 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)	3020417125
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	2001 Sanyo Avenue Suite 130 San Diego, CA, US 92154
Registration status	Active · expires 2026
Parent company	CODAN US Corporation (owner-operator 8010060)
Brand names	CODAN

Activity by year

Recalls (2)

Devices registered here (1)

Set, Administration, Intravascular
Product code FPA (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5440

Recalls & enforcement

Class IITerminated2019-09-12
Individual packages of connectors may have incomplete or bad seals which would compromise sterility.
Class IITerminated2011-08-17
CODAN US Corporation is recalling the ColorSafe IV (intravenous) product lines because they were manufactured and marketed prior to FDA approval.

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. “CODAN US Corporation (FEI 3020417125) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3020417125-codan-us-corporation/

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