Lower risk Medical device recall · FDA · Published August 21, 2024

Percussionaire IPV Therapy In-Line Valve Recall: Blue Cap Removal Required

Percussion: Percussionaire recalls 20 IPV therapy in-line valves with specific serial numbers due to updated labeling requirements for blue cap removal before use.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-3208-2024Medical device Percussionaire ›

Lower-risk recall

Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.

Take action

Contact the company

Recalling firmPercussionaire Corporation130 Mcghee Rd Ste 109 · Sandpoint, ID 83864-8409

✎ GovInfoNow plain-language explainer

Percussionaire is recalling 20 IPV therapy in-line valves that require the blue cap on the in-line valve to be removed before use. This recall is due to updated labeling instructions to ensure safe delivery of IPV therapy. Read more at govinfonow.com/recall/54182-percussionaire-ipv-therapy-in-line-valve-recall-blue-cap-removal.

Source Summary by GovInfoNow · govinfonow.com/recall/54182-percussionaire-ipv-therapy-in-line-valve-recall-blue-cap-removal · Updated August 19, 2026 · FDA enforcement record: FDA #Z-3208-2024

Cite this page

“Percussionaire IPV Therapy In-Line Valve Recall: Blue Cap Removal Required.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54182-percussionaire-ipv-therapy-in-line-valve-recall-blue-cap-removal. Based on FDA recall #Z-3208-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3208-2024%22&limit=1).

The FDA announced on Aug. 21, 2024, that Percussionaire Corporation is recalling its IPV therapy In-Line Valve due to labeling issues. The company updated the labeling to ensure the blue cap on the in-line valve is removed prior to delivery of therapy.

How to tell if you have it

Brand: Percussionaire
Product: Percussionaire, Inc., REF: P5-TEE-20, IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve
Lots: 240620 240610 240418 240326 230612 WO07066 WO07010 WO06020 WO05019 WO04884 WO04827 WO04756 WO04714 WO04656 WO04625 WO04596 WO04553 WO04398 WO04356 WO04061 WO03846 WO03748 WO03688
Quantity: 2523 units

The hazard

According to the FDA, the hazard involves updated labeling to ensure that the blue cap on the in-line valve is removed prior to delivery of Intrapulmonary percussive ventilation (IPV) therapy.

Context

GovInfoNow's records show Percussionaire Corporation has 7 other recalls on record since Sept. 14, 2020. Other recent recalls of similar products include Bard PowerMidline Catheter Recall: Lidocaine Ampoules Deficient Manufacturing (May 21, 2026) and Bard Poly Midline Catheters Recall: Lidocaine Ampoules Deficient Manufacturing (May 21, 2026).

How to tell if you have this one

Check the serial numbers listed: 240620, 240610, 240418, 240326, 230612, WO07066, WO07010, WO06020, WO05019, WO04884, WO04827, WO04756, WO04714, WO04656, WO04625, WO04596, WO04553, WO04398, WO04356, WO04061, WO03846, WO03748, WO03688.

Brand
Percussionaire
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class I
Status
Ongoing
Distribution
US: Nationwide OUS: Israel Japan Russia Switzerland Canada Turkey

Recall number	Product, codes & lots	Quantity
Z-3207-2024	Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve; No UDI/ Lots: 240620, 240610, 240418, 240326, 230612, WO07066, WO07010, WO06020, WO05019, WO04884, WO04827, WO04756, WO04714, WO04656, WO04625, WO04596, WO04553, WO04398, WO04356, WO04061, WO03846, WO03748, WO03688	50,460 units
Z-3208-2024	Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve; No UDI/Lots: 240620 240610 240418 240326 230612 WO07066 WO07010 WO06020 WO05019 WO04884 WO04827 WO04756 WO04714 WO04656 WO04625 WO04596 WO04553 WO04398 WO04356 WO04061 WO03846 WO03748 WO03688	2523 units

Based on the official FDA remedy

What to do — step by step

Check Serial Numbers
Verify your device's serial numbers against the list provided in the recall notice.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “US: Nationwide OUS: Israel Japan Russia Switzerland Canada Turkey” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 49 days after the firm started it.

Aug 21, 2024Firm started the recall
Sep 27, 2024FDA classified it Class I
Oct 9, 2024Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

What should I do if I have this device?

Check your device's serial numbers against the list provided in the recall notice. No immediate action is required beyond verifying the serial numbers.

Is there a risk of injury from this device?

The recall addresses a labeling requirement for safe use, not a direct risk of injury. The hazard level is low risk.

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Link to this recall

<a href="https://govinfonow.com/recall/54182-percussionaire-ipv-therapy-in-line-valve-recall-blue-cap-removal">Percussionaire IPV Therapy In-Line Valve Recall: Blue Cap Removal Required (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-3208-2024 (August 21, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3208-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.