Reported Oct 7, 2026 · Ongoing · Updated Oct 13, 2026
Impulsator, Product Number: S00010, Phasitron 5, Product Number: P5 used with Instruction Manual
Percussionaire Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Percussionaire Corporation · 130 Mcghee Rd Ste 109 · Sandpoint, ID · 83864-8409
Is this the product you have?
- Impulsator
- Product Number
S00010Phasitron 5
- Product NumberP5 used with Instruction Manual
- Lot codes and dates
- Product Number/UDI-DI
S00010/00849436000389P5/00849436000501
- Instruction ManualP20047 Rev E
- Product Number/UDI-DI
- Amount recalled
- 228,277
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
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
This product could cause temporary or reversible health problems — stop using it.
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