# FDA recall Z-0637-2024

> **Percussionaire Corporation** · Class I · device recall initiated 2023-12-12.

## Product

High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123

## Reason for recall

Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe  impact to the end user

## Distribution

US:AL	AR	CA	CT	FL	GA	IL	IN	KS	LA	MI	MN	MO	NC	NJ	OH	OR	TN	TX	UT	VA OUS: None

## Key facts

- **Recall number:** Z-0637-2024
- **Recalling firm:** Percussionaire Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-12
- **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-0637-2024

## Citation

> AI Analytics. FDA recall Z-0637-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0637-2024. Source: US FDA. Licensed CC0.

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