Facility

AMETEK Lamb Motores de Mexico, S. de R.L. de C.V.

2 recall(s) on record — most severe on record: Class II.

Key facts

2recalls · 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)	3002894792
Establishment type	Manufacture Medical Device
Location	Avenida Rio San Juan SN Reynosa Tamaulipas, MX 88730
Registration status	Active · expires 2026
Parent company	REICHERT INC. (owner-operator 9055850)
Brand names	Tono-Vera® Tonometer Starter Kit, Rechargeable; Ocu-Dot® Tonometer Probes - 100 Count; Tono-Vera® Tonometer Starter Kit, AA Battery

Activity by year

Recalls (2)

Devices registered here (1)

Tonometer, Manual
Product code HKY (opens in a new tab) · Class II · Ophthalmic · 21 CFR 886.1930

Recalls & enforcement

Class IIOngoing2025-02-28
The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Class IIOngoing2023-07-20
Phoroptor VRx Head may detach from the bracket that connects the Phoroptor VRx Head to an ophthalmic stand. If the Phoroptor VRx Head detaches from the bracket, it can fall onto a patient or device operator

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. “AMETEK Lamb Motores de Mexico, S. de R.L. de C.V. (FEI 3002894792) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002894792-ametek-lamb-motores-de-mexico-s-de-r-l-d/

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