FDA Device Intelligence
Home › Ventec Life Systems, Inc. › VOCSN Humidifier Bypass

VOCSN Humidifier Bypass

Ventec Life Systems, Inc. · Model Blue · UDI-DI 00855573007136

NHJNOUCBK
1
510(k) clearances
201
Adverse events (11 deaths)
17
Recalls
29
Facilities

Description

VOCSN Humidifier Bypass (Blue) Available as - 10-pack (00855573007372) - 4-Pack of Humidifier Bypass (00855573007136) with 4-pack of Adult, Active, Heated, Blue Circuit (00855573007921)

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

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.