# FDA recall Z-1444-2023

> **Draeger Medical, Inc.** · Class I · device recall initiated 2023-04-17.

## Product

VentStar Anesthesia WT (P)180, MP00374

## Reason for recall

Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

## Distribution

Domestic: US Nationwide Distribution.

## Key facts

- **Recall number:** Z-1444-2023
- **Recalling firm:** Draeger Medical, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2023-04-17
- **Report date:** 2023-05-24
- **Termination date:** 2024-09-03

- **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-1444-2023

## Citation

> AI Analytics. FDA recall Z-1444-2023. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1444-2023. Source: US FDA. Licensed CC0.

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