Facility

ACCUTRON, INC.

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

Key facts

1recalls · worst Class I

—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)	2020813
Establishment type	Manufacture Medical Device
Location	1625 W Pinnacle Peak Rd PHOENIX, AZ, US 85027
Registration status	Active · expires 2026
Parent company	Accutron Inc (owner-operator 2020813)
Brand names	TUBING, PRESSURE AND ACCESSORIES

Activity by year

Recalls (1)

Devices registered here (1)

Tubing, Pressure And Accessories
Product code BYX (opens in a new tab) · Class I · Anesthesiology · 21 CFR 868.5860

Recalls & enforcement

Class ITerminated2012-04-29
Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it flows Nitrous Gas without Oxygen gas being turned on, it functions in an incorrect manner.

All facilities operated by Accutron Inc

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. “ACCUTRON, INC. (FEI 2020813) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2020813-accutron-inc/

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