# FDA recall Z-0739-2019

> **Draeger Medical, Inc.** · Class I · device recall initiated 2018-12-21.

## Product

VentStar Basic (P) 250, Catalog Number MP00352     Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only. Breathing Circuits/Anesthesia Sets with Water trap: Breathing circuit for conveying breathing gases between an anesthesia delivery system or ventilator and a pediatric patient. Intended for single use only. Water traps are intended for collection of condensate. The standard breathing circuit is equipped with a water trap in each breathing hose limb.

## Reason for recall

Incorrectly pre-assembled breathing circuit has potential for incorrect connection/short circuit of the breathing circuit

## Distribution

US Distribution to states of: AL, CA, CO, CT, FL, KY, MI, NJ, OH, PA, SC & TX.

## Key facts

- **Recall number:** Z-0739-2019
- **Recalling firm:** Draeger Medical, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-12-21
- **Report date:** 2019-01-30
- **Termination date:** 2019-04-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Telford, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0739-2019

## Citation

> AI Analytics. FDA recall Z-0739-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0739-2019. Source: US FDA. Licensed CC0.

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