Facility

A-M Systems

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)	3020614
Establishment type	Repack or Relabel Medical Device
Location	131 BUSINESS PARK LOOP Sequim, WA, US 98382
Registration status	Active · expires 2026
Parent company	A-M SYSTEMS, LLC (owner-operator 3020614)
Brand names	ABSORBER; CARBON DIOXIDE

Activity by year

Recalls (1)

Devices registered here (1)

Absorber, Carbon-Dioxide
Product code BSF (opens in a new tab) · Class I · Anesthesiology · 21 CFR 868.5310

Recalls & enforcement

Class IITerminated2018-08-10
Some of the Disposable Smooth Interior Tubing may pull apart when stretched.

All facilities operated by A-M SYSTEMS, LLC

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. “A-M Systems (FEI 3020614) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3020614-a-m-systems/

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