Official recall record
Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to provide airway clearance
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-09-16
- Country of alert
- United States
- Alert level
- Class I
- Alert type
- recall
- Brand on record
- Percussionaire Corporation
What the authority reported
As a result of product complaints, breathing circuits are experiencing discolored fluid which are formed when therapy was being given with specific medication through the nebulizer cup. Discoloration is caused by a reaction between medicated mist and an inadvertent/unapproved addition of a nickel coating on the spring component.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2026-08-18 · US FDA — Medical Devices
Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with Instruction Manual - 2026-08-18 · US FDA — Medical Devices
Intrapulmonary Percussive Ventilation, IPV-2C, Product Number: S00002-C; Phasitron 5, Product Number: P5 used - 2026-08-18 · US FDA — Medical Devices
Travel Air, Product Number: S00055; Phasitron 5, Product Number: P5 used with Instruction Manual
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