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The Vest APX System

HILL-ROM SERVICES PTE. LTD. · Model M08368W · UDI-DI 00887761008045

NHJ Prescription
10
510(k) clearances
201
Adverse events (11 deaths)
17
Recalls
29
Facilities

Description

Home Care packaging for The Vest APX, WAR

Recalls

DateFirmReason
2026-08-18Percussionaire CorporationLabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o
2026-08-18Percussionaire CorporationLabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o
2026-08-18Percussionaire CorporationLabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o
2026-08-18Percussionaire CorporationLabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o
2026-08-18Percussionaire CorporationLabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o
2026-08-18Percussionaire CorporationLabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery o
2026-08-03Baxter Healthcare CorporationContamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to firm and testing confirmed devi
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

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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.