Class II — Percussionaire Corporation
| Recalling firm | PERCUSSIONAIRE CORP. |
|---|---|
| Registered facility | PERCUSSIONAIRE CORP. (the firm's only registered facility) |
| Classification | Class II |
| Status | Completed |
| Reason | Note this recall occurred in 2020 and 2021. Reports of screen freeze on visual displays of waveform analyzers that are paired with ventilators. Subsequently, waveform analyzers were serviced to install PAL microprocessor chips and firmware. |
| Product | Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators. |
| Quantity | 212 |
| Distribution | US: CA, ND, MS, MD |
| Initiated | 2020-09-14 |
| Classified | 2023-11-07 |
| Recall number | Z-0259-2024 |
| 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 II recall — Percussionaire Corporation (Z-0259-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93192/
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