Facility

ON SITE GAS SYSTEMS, INC.

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

Key facts

1recalls · worst Class II

3inspections · worst VAI

—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)	3003637574
Establishment type	Manufacture Medical Device
Location	35 Budney Rd Newington, CT, US 06111
Registration status	Active · expires 2026
Parent company	ON SITE GAS SYSTEMS, INC. (owner-operator 9096051)
Brand names	POGS; POGS33C; POGS33

Activity by year

Recalls (1)
Inspections (3)

Devices registered here (1)

Generator, Oxygen, Portable
Product code CAW (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.5440

Recalls & enforcement

Class IITerminated2013-12-19
Heat exchanger hose becomes weak and may fail.

FDA inspections (3)

NAI2024-05-15
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
VAI2019-03-14
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
VAI2017-10-03
Voluntary Action Indicated · Compliance: Devices · citations posted

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.

All facilities operated by ON SITE GAS SYSTEMS, 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. “ON SITE GAS SYSTEMS, INC. (FEI 3003637574) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003637574-on-site-gas-systems-inc/

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