Percussion: Percussionaire recalls 20 IPV therapy in-line valves with specific serial numbers due to updated labeling requirements for blue cap removal before use.
Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy.
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.
The blue cap on the in-line valve must be removed before delivering IPV therapy. If not removed, the device may not function correctly, potentially affecting treatment effectiveness.
Patients using Percussionaire's IPV therapy in-line valves with specific serial numbers (listed in the recall) are affected. Healthcare providers who administer these devices are most at risk.
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.
Verify your device's serial numbers against the list provided in the recall notice.
The recall is due to updated labeling requirements that specify the blue cap on the in-line valve must be removed before delivering IPV therapy.
Check your device's serial numbers against the list provided in the recall notice. No immediate action is required beyond verifying the serial numbers.
The recall addresses a labeling requirement for safe use, not a direct risk of injury. The hazard level is low risk.
We’ve drafted a message you can send Percussionaire to request your refund or repair — edit it as you like.
Subject: Recall Z-3208-2024 — Percussionaire Percussionaire Hello, I own a Percussionaire that is covered by recall Z-3208-2024 from Percussionaire. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
