Percussionaire Corporation 2025-01-29 Health critical FDA
Health · FDA · Recall #FDA-Z-0960-2025
VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D… Recall
Issued January 29, 2025 · Percussionaire Corporation
In January 2025, Percussionaire Corporation recalled the VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation.
What you should do
- 1 Stop using VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Percussionaire Corporation to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Percussionaire Corporation
- Category
- Health
- Recall date
- January 29, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - U.S. Nationwide distribution in the states of AZ, FL, IL, MS, MO, NE, NJ, NY, NC, RI, TX, UT, and WV. The countries of Belgium,
- Recall number
- FDA-Z-0960-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Percussionaire Corporation has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.