Percussionaire recalls High Frequency Transport Phasitron Breathing Circuit Kit REF A50605-D (Rx Only) due to assembly errors causing potential severe pressure output issues. Affected units have specific lot numbers and were sold with CE 0123 marking.
Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe impact to the end user
Percussionaire is recalling a high-frequency breathing circuit kit that may have assembly errors causing dangerous pressure output. This could lead to severe harm to patients using the device. Affected units have specific lot numbers and were sold with CE 0123 marking.
The breathing circuit kit has an assembly error that can cause its pressure output to be affected. This may result in severe impacts to the end user, meaning patients could experience serious harm from the device.
Healthcare professionals using the Percussionaire High Frequency Transport Phasitron Breathing Circuit Kit for medical purposes are most at risk. Patients receiving treatment with this device could be harmed by the pressure issues.
Check for the model REF: A50605-D (Rx Only) with CE 0123 marking. Affected units have specific lot numbers: WO05216, WO05254, WO05321, WO05392, WO05559, WO05588, WO05684, WO05749, WO05896, WO05930, WO06028.
Immediately stop using the Percussionaire High Frequency Transport Phasitron Breathing Circuit Kit if it has the affected lot numbers listed.
No, Percussionaire has recalled this product due to assembly errors that can cause dangerous pressure output, so it should not be used.
Affected lot numbers are WO05216, WO05254, WO05321, WO05392, WO05559, WO05588, WO05684, WO05749, WO05896, WO05930, and WO06028.
Check for the model REF: A50605-D (Rx Only) with CE 0123 marking and the specific lot numbers listed in the recall.
We’ve drafted a message you can send Percussionaire to request your refund or repair — edit it as you like.
Subject: Recall Z-0637-2024 — Percussionaire Percussionaire Hello, I own a Percussionaire that is covered by recall Z-0637-2024 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.
