# FDA recall Z-0693-2024

> **Percussionaire Corporation** · Class I · device recall initiated 2023-03-28.

## Product

Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)

## Reason for recall

Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.

## Distribution

US: RI, CA, TX

## Key facts

- **Recall number:** Z-0693-2024
- **Recalling firm:** Percussionaire Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-28
- **Report date:** 2024-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sandpoint, ID, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0693-2024

## Citation

> AI Analytics. FDA recall Z-0693-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0693-2024. Source: US FDA. Licensed CC0.

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