Facility

KIMBERLY-CLARK CORPORATION PARIS PLANT

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)	3002614014
Establishment type	Manufacture Medical Device
Location	2466 Farm Road 137 PARIS, TX, US 75460
Registration status	Active · expires 2026
Parent company	KIMBERLY-CLARK CORPORATION (owner-operator 9001775)
Brand names	Speax; Poise; Depend; goodnites; Thinx

Activity by year

Recalls (1)

Devices registered here (1)

Garment, Protective, For Incontinence
Product code EYQ (opens in a new tab) · Class I · Gastroenterology, Urology · 21 CFR 876.5920

Recalls & enforcement

Class IITerminated2018-12-11
Potential for tampon to come apart upon removal.

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. “KIMBERLY-CLARK CORPORATION PARIS PLANT (FEI 3002614014) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002614014-kimberly-clark-corporation-paris-plant/

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