Distal Phasitron — Class I medical device recall Z-0693-2024
Ongoing recall by Percussionaire Corporation, reported 2024-01-24, distributed in CA, RI, TX. Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than
| Recall number | Z-0693-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Percussionaire Corporation, Sandpoint, ID, United States |
| Recall initiated | 2023-03-28 |
| Classified | 2024-01-17 |
| Reported by FDA | 2024-01-24 |
| Distributed | CA, RI, TX |
| Quantity | 195 |
| UPC / GTIN / UDI-DI | 00849436000693 |
| Lot numbers | WO03739, WO04218 |
| Model numbers | S20020 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0693-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.