# FDA recall Z-2434-2020

> **Westmed, Inc.** · Class II · device recall initiated 2019-01-15.

## Product

Neo-Vent Infant T-Piece Resuscitation Circuit;Circuit for use on compatible Infant Resuscitators. 15mm OD x 10mm ID connector; REF 0415, Qty:10, Length: 60" (1.5cm), Rx Only.

## Reason for recall

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.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of CA, GA, IL,OH, MA, MI, MO, NC, OH, OR, TX, VA, and WI. The country of Spain.

## Key facts

- **Recall number:** Z-2434-2020
- **Recalling firm:** Westmed, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-15
- **Report date:** 2020-07-08
- **Termination date:** 2021-02-05

- **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-2434-2020

## Citation

> AI Analytics. FDA recall Z-2434-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2434-2020. Source: US FDA. Licensed CC0.

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