Recall Register

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Percussionaire Corporation

FDA recalling firm · 7 enforcement events · 8 product records · 2020–2025 · ID

Percussionaire Corporation has 7 FDA enforcement events on this register (8 product records) between 2020 and 2025: 7 device; the busiest year was 2024 with 3.

86% of its events are Class I; the most common class is Class I (6). 6 events are listed as ongoing; the recalling firm's address is in ID.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
17 Sep 2025Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for UseDeviceClass I1Ongoing
23 Dec 2024VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single Patient, 5pk -A51001, VDR4 Control Unit Tester -PRT 991, VDR W/SWIVEL T SINGLE PATIENT PHASITRON -PRT 992, VDR4 HUMIDIFICATION ADAPTER KIT, CASE OF 10 -PRT 993, VDR4 Humidification Kit with Cross Tee,…DeviceClass I1Ongoing
16 Sep 2024Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to provide airway clearance therapyDeviceClass I1Ongoing
21 Aug 2024Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line ValveDeviceClass I2Ongoing
12 Dec 2023High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123DeviceClass I1Ongoing
28 Mar 2023Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)DeviceClass I1Ongoing
14 Sep 2020Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators.DeviceClass II1Completed

By type and class

Device7
Class I6
Class II1

Class I: 86% of this firm's events; 18% of all events on the register.

Events by year

20
21
22
23
24
25
26
Enforcement events for Percussionaire Corporation by year initiated.

Questions and answers

How many FDA recalls has Percussionaire Corporation had?

7 enforcement events (8 product records) on this register, 2020–2025: 7 device.

Are any Percussionaire Corporation recalls ongoing?

6 events are listed as ongoing in the current openFDA export.

What class are Percussionaire Corporation recalls?

6 Class I, 1 Class II. 86% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.