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Medtronic Perfusion Systems alerts
Verified recalls, refunds, lawsuits, and settlements involving Medtronic Perfusion Systems.
Recall
Active
FDA
Official source
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation,...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister,...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Certain lots of product have the potential for a sterile barrier breach. Product details: Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Certain lots of product have the potential for a sterile barrier breach. Product details: Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T;...
- Company
- Medtronic Perfusion Systems
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration