Medtronic Perfusion Systems 2025-09-10 Health critical FDA
Health · FDA · Recall #FDA-Z-2481-2025
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT… Recall
Issued September 10, 2025 · Medtronic Perfusion Systems
In September 2025, Medtronic Perfusion Systems recalled the DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT…, 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
The catheters may not retain their shape.
What you should do
- 1 Stop using DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medtronic Perfusion Systems 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
- Medtronic Perfusion Systems
- Category
- Health
- Recall date
- September 10, 2025
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution.
- Recall number
- FDA-Z-2481-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Medtronic Perfusion Systems has 11 recalls in our database, including 2 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.