FDA Device Intelligence
HomePERCUSSIONAIRE CORPORATION › Percussionaire

Percussionaire

PERCUSSIONAIRE CORPORATION · Model P5 · UDI-DI 00849436000686

NHJ Prescription
1
510(k) clearances
189
Adverse events (11 deaths)
10
Recalls
29
Facilities

Description

Phasitron 5 With Unified Connector

Recalls

DateFirmReason
2026-05-21Baxter Healthcare CorporationThere have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the
2026-05-21Baxter Healthcare CorporationThere have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the
2026-05-21Baxter Healthcare CorporationThere have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the
2026-05-21Baxter Healthcare CorporationThere have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the
2026-02-18Baxter Healthcare CorporationUrgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen l
2024-09-16Percussionaire CorporationAs 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
2024-05-30Baxter Healthcare CorporationPotential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow
2024-05-30Baxter Healthcare CorporationPotential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow
2022-04-26Baxter Healthcare CorporationThere is a potential of reduced oxygenation or pneumothorax/barotrauma to occur when the Volara system is used with in-line ventilator in home care environment.
2022-04-26Baxter Healthcare CorporationThere is a potential of reduced oxygenation or pneumothorax/barotrauma to occur when the Volara system is used with in-line ventilator in home care environment.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.