FDA Device recall Z-0693-2024
Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
- FDA Device
- Class I
- ongoing
- Published 2024-01-24
On 2024-01-24 the FDA classified a Class I recall of Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit) by Percussionaire, citing breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0693-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-03-28 |
| Published | 2024-01-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Percussionaire |
| Distribution | CA, RI, TX |
Product
Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
Reason
Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.
Identifiers
| code_info | UDI-DI: 00849436000693, Lots/Expiration: WO03739/September 13, 2024, and WO04218/November 14, 2024. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0693-2024%22
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