Percussionaire recalls
Percussionaire has 15 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 7 Oct 2026. 14 are still ongoing. 7 were reported in the last 12 months.
Total recalls15since 2023
Last 12 months7reported
Class I747% of total
Ongoing14latest 7 Oct 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 7 47%Class II 8 53%Class III 0 0%
Why percussionaire is recalled
Product types
By year
Ongoing percussionaire recalls
14 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065 recalled | Percussionaire | Other | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV-1C recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Travel Air, Product Number: S00055 recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Impulsator, Product Number: S00010, Phasitron recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | In-Line Valve, Product Number: P5-TEE recalled by Percussionaire | Percussionaire | Other | Nationwide |
| Device | CLASS II | Intrapulmonary Percussive Ventilation, IPV-2C recalled by Percussionaire | Percussionaire | Other | Nationwide |
All percussionaire recalls, newest first
15 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.