Facility

LIDCO LTD.

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)	3001139253
Establishment type	Manufacture Medical Device
Location	Unit D4 LONDON England, GB N17 0QJ
Registration status	Active · expires 2026
Parent company	LIDCO LTD. (owner-operator 9036223)
Brand names	LiDCOplus Hemodynamic Monitor

Activity by year

Recalls (1)

Devices registered here (1)

Computer, Diagnostic, Pre-Programmed, Single-Function
Product code DXG (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.1435

Recalls & enforcement

Class IITerminated2020-11-19
The expiration date on labeling is incorrect.

All facilities operated by LIDCO 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. “LIDCO LTD. (FEI 3001139253) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3001139253-lidco-ltd/

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