Facility

POSEY, S. de R.L. de C.V.

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)	3002563411
Establishment type	Manufacture Medical Device
Location	AVENIDA FERROCARRIL #16901 INT: 64, COL. RIO TIJUANA Baja California, MX 22226
Registration status	Active · expires 2026
Parent company	TIDI PRODUCTS, LLC (owner-operator 2020362)
Brand names	Posey

Activity by year

Recalls (1)

Devices registered here (1)

Monitor, Bed Patient
Product code KMI (opens in a new tab) · Class I · General Hospital · 21 CFR 880.2400

Recalls & enforcement

Class IITerminated2019-04-12
Not meeting design specifications.

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. “POSEY, S. de R.L. de C.V. (FEI 3002563411) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002563411-posey-s-de-r-l-de-c-v/

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