medical MODERATE Updated 2026-10-07

Percussionaire Corporation recalls In-Line Valve, Product Number: P5-TEE

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Recalled Product

In-Line Valve, Product Number: P5-TEE

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: 00849436000723

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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