Percussionaire recalls IPV therapy in-line valves with specific serial numbers due to updated labeling requirements for blue cap removal before therapy delivery.
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 a single IPV therapy in-line valve model for updated labeling. The recall requires removing the blue cap before use to ensure safe delivery of IPV therapy.
The blue cap on the in-line valve must be removed before delivering IPV therapy. Failure to remove it could lead to improper therapy delivery, though the hazard is not described as causing serious injury in normal use.
Healthcare providers using Percussionaire's IPV therapy in-line valves for medical treatment. Patients receiving IPV therapy through this device are most at risk if the blue cap is not removed.
Check for serial numbers: 240620, 240610, 240418, 240326, 230612, WO07066, WO07010, WO06020, WO05019, WO04884, WO04827, WO04756, WO04714, WO04656, WO04625, WO04596, WO04553, WO04398, WO04356, WO04061, WO03846, WO03748, WO03688. This valve is only available by prescription.
Verify the valve's serial number against the list: 240620, 240610, 240418, 240326, 230612, WO07066, WO07010, WO06020, WO05019, WO04884, WO04827, WO04756, WO04714, WO04656, WO04625, WO04596, WO04553, WO04398, WO04356, WO04061, WO03846, WO03748, WO03688.
Ensure the blue cap is removed before using the valve for IPV therapy delivery.
The recall requires removing the blue cap before delivering IPV therapy to ensure proper labeling and safe use.
The affected serial numbers are: 240620, 240610, 240418, 240326, 230612, WO07066, WO07010, WO06020, WO05019, WO04884, WO04827, WO04756, WO04714, WO04656, WO04625, WO04596, WO04553, WO04398, WO04356, WO04061, WO03846, WO03748, WO03688.
Yes, but the blue cap must be removed before use to ensure safe delivery of IPV therapy.
We’ve drafted a message you can send Percussionaire to request your refund or repair — edit it as you like.
Subject: Recall Z-3207-2024 — Percussionaire Percussionaire Hello, I own a Percussionaire that is covered by recall Z-3207-2024 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.
