Class I — Percussionaire Corporation
| Recalling firm | PERCUSSIONAIRE CORP. |
|---|---|
| Registered facility | PERCUSSIONAIRE CORP. (the firm's only registered facility) |
| Classification | Class I |
| Status | Ongoing |
| Reason | Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy. |
| Product | Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit) |
| Quantity | 195 |
| Distribution | US: RI, CA, TX |
| Initiated | 2023-03-28 |
| Classified | 2024-01-17 |
| Recall number | Z-0693-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — Percussionaire Corporation (Z-0693-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93648/
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