ClearanceBrief
Recall Z-2217-2026 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Medtronic Perfusion Systems

Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter

DateMay 20, 2026 (initiated Apr 21, 2026)
StatusOpen, Classified
ReasonCertain lots of product have the potential for a sterile barrier breach.
Root causePackaging process control
ActionMedtronic Cardiac Surgery issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 4/21/2026 via UPS. The notice explained the issue, potential risk. and requested that the affected product be returned by contacting Customer Service at 1-800-854-3570, Option 1 then Option 4, and referencing this communication to initiate return for credit or replacement product. Consignees were directed to share this notification with others in your organization as appropriate. If the product listed above has been forwarded to another facility, please notify the facility. For questions regardin
Quantity840 units
DistributionWorldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, S
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K860149VENOUS PERFUSION CANNULA W/CUFF CAT. NO. 94015
Dlp, Inc., Mar 31, 1986
K953945RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLET
Dlp, Inc., Mar 26, 1996