FDA recall record

Percussionaire High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx recall — FDA Z-0637-2024

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…

Class Iclassification
Z-0637-2024official record ID
Jan 24, 2024report date

Recall record at a glance

Official recordZ-0637-2024
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmPercussionaire Corporation
Report dateJan 24, 2024
Recall initiation dateDec 12, 2023
Quantity2145 units
LocationSandpoint, ID, United States

Official product description

High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123

Why the product was recalled

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

Distribution information

US:AL AR CA CT FL GA IL IN KS LA MI MN MO NC NJ OH OR TN TX UT VA OUS: None

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

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Percussionaire recall — FDA Z-3207-2024

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

Class IFDA: OngoingPercussionaire Corporation