Facility

PHASOR HEALTH, LLC

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)	3016577622
Establishment type	Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Location	8944 Kirby Drive Houston, TX, US 77054
Registration status	Active · expires 2026
Parent company	Phasor Health, LLC (owner-operator 10062497)
Brand names	EVAC

Activity by year

Recalls (1)

Devices registered here (1)

Shunt, Central Nervous System And Components
Product code JXG (opens in a new tab) · Class II · Neurology · 21 CFR 882.5550

Recalls & enforcement

Class IIOngoing2025-03-21
Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.

All facilities operated by Phasor Health, 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. “PHASOR HEALTH, LLC (FEI 3016577622) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3016577622-phasor-health-llc/

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