RecallRadar

FDA Device recall Z-3319-2026

Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065

On 2026-10-07 the FDA classified a Class II recall of Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065 by Percussionaire, citing labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3319-2026
ClassificationClass II
Statusongoing
Initiated2026-08-18
Published2026-10-07
Last updated2026-10-13 05:30 UTC
CompanyPercussionaire
DistributionUS

Product

Intrapulmonary Percussive Ventilation, IPV 1, Product Number: S00065; Phasitron 5 Breathing Circuit with Unified Connector, Product Number: P5-UC, used with In-Line Valve Instruction Manual

Reason

Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation

Identifiers

code_infoProduct Number/UDI-DI: S00065/00849436000679, 00849436000709; P5-UC/00849436000686 In-Line Valve Instruction Manual: P20174 Rev D

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-13 05:30 UTC. Current status: ongoing.

Other recalls by Percussionaire

All Percussionaire recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3319-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.