Facility

T.G. EAKIN, LTD.

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

Key facts

1recalls · worst Class III

—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)	1000339531
Establishment type	Manufacture Medical Device
Location	15 BALLYSTOCKART RD. COMBER, COUNTY DOWN Ards and North Down, GB BT23 5QY
Registration status	Active · expires 2026
Parent company	T.G. EAKIN, LTD. (owner-operator 9014145)
Brand names	Eakin Cohesive Paste; Eakin Cohesive Skin Barriers; Eakin Cohesive Seals; Eakin Freeseal

Activity by year

Recalls (1)

Devices registered here (1)

Protector, Ostomy
Product code EXE (opens in a new tab) · Class I · Gastroenterology, Urology · 21 CFR 876.5900

Recalls & enforcement

Class IIIOngoing2024-08-08
On lot of cartons of Eakin Cohesive small seals, Model Number 839002 may contain blistered seals labelled as 839005.

All facilities operated by T.G. EAKIN, 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. “T.G. EAKIN, LTD. (FEI 1000339531) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000339531-t-g-eakin-ltd/

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