Westmed Javid de Mexico, S.A. de C.V.

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

Devices registered here (1)

• Flowmeter, Calibration, Gas
  Product code BXY · Class I · Anesthesiology · 21 CFR 868.2350

Recalls & enforcement

• Class IIOngoing2024-09-27
  Due to connector within the circuit flex extender not meeting specifications resulting in a low connection force and as a result, the connector may leak or disconnect and may cause life threating conditions or death.
• Class IITerminated2020-11-11
  There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
• Class IITerminated2019-01-15
  A repair was made to an adapter mold resulting in parts being produced with compliant 10mm ID connections and non-compliant 15mm OD connections. This resulted in facilities with infant resuscitators that connect via the 15mm OD fitting not being able to use those circuits.
• Class IITerminated2011-01-18
  Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.

Related

• All facilities operated by WESTMED, INC.

Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →