Facility

ALPHA OMEGA ENGINEERING LTD.

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)	3001610756
Establishment type	Manufacture Medical Device
Location	Hamerkava St. 6 Nof HaGalil Northern, IL 17890
Registration status	Active · expires 2026
Parent company	ALPHA OMEGA ENGINEERING LTD. (owner-operator 9039414)
Brand names	Sterile NeuroProbe; Sterile Electrode Cable; Sterile Cannula

Activity by year

Recalls (1)

Devices registered here (1)

Electrode, Depth
Product code GZL (opens in a new tab) · Class II · Neurology · 21 CFR 882.1330

Recalls & enforcement

Class ITerminated2018-09-04
If cables are improperly connected, current may reach high charge density, causing tissue harm.

All facilities operated by ALPHA OMEGA ENGINEERING LTD.

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. “ALPHA OMEGA ENGINEERING LTD. (FEI 3001610756) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3001610756-alpha-omega-engineering-ltd/

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