FDA Enforcement Class II Terminated

Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK, REF 3228-e, RX Only, CE0482, (01)10709078008020 - Product Usage: intended to connect with an oxygen source to deliver oxygen therapy to the patient.

Recall: Z-0742-2021 · Reported January 6, 2021

Enforcement

Recall Number
Z-0742-2021
Event ID
86903
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Westmed, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
January 6, 2021
Initiation Date
November 11, 2020
Classification Date
December 29, 2020
Termination Date
February 7, 2023
Address
5580 S Nogales Hwy Ste 170, N/A, Tucson, AZ, 85706-3333, United States

Description

Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK, REF 3228-e, RX Only, CE0482, (01)10709078008020 - Product Usage: intended to connect with an oxygen source to deliver oxygen therapy to the patient.

Reason

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.

Code Info

Lot # 081120N42, 090220N29, 091020N88

Distribution

Worldwide distribution - US Nationwide distribution including in the states of PA, OK, MO, CO, RI, IL, CA, TX, OH, MD, IL, MN, KS and the countries of Canada, Korea, United Kingdom

Quantity

37,300 units