RecallRadar

FDA Device recall Z-3320-2026

In-Line Valve, Product Number: P5-TEE

On 2026-10-07 the FDA classified a Class II recall of In-Line Valve, Product Number: P5-TEE 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-3320-2026
ClassificationClass II
Statusongoing
Initiated2026-08-18
Published2026-10-07
Last updated2026-10-13 05:30 UTC
CompanyPercussionaire
DistributionUS

Product

In-Line Valve, Product Number: P5-TEE

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_infoUDI: 00849436000723

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-3320-2026%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.