Medtronic Perfusion Systems 2026-05-27 Health serious FDA
Health · FDA · Recall #FDA-Z-2218-2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725;… Recall
Issued May 27, 2026 · Medtronic Perfusion Systems
In May 2026, Medtronic Perfusion Systems recalled the Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725;…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Certain lots of product have the potential for a sterile barrier breach.
What you should do
- 1 Stop using Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725;… 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
- May 27, 2026
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmar
- Recall number
- FDA-Z-2218-2026
- 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 356th Health recall we've logged in 2026.