# FDA recall Z-0741-2021

> **Westmed, Inc.** · Class II · device recall initiated 2020-11-11.

## Product

REF 3102-E, Elongated Oxygen Mask, Adult Oxygen Elongated Mask with 8' Tubing, Rx Only, CE0482, (01)00709078003172 - Product Usage: intended to connect with an oxygen source to deliver oxygen therapy to the patient.

## Reason for recall

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.

## 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

## Key facts

- **Recall number:** Z-0741-2021
- **Recalling firm:** Westmed, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-11-11
- **Report date:** 2021-01-06
- **Termination date:** 2023-02-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tucson, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0741-2021

## Citation

> AI Analytics. FDA recall Z-0741-2021. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0741-2021. Source: US FDA. Licensed CC0.

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