Home/Recalls/FDA-Z-2214-2026
FDA DevicesClass II

Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model...

Published: May 27, 2026Recall ID: Z-2214-2026Category: devicesCountry: US

Reason for Recall / Hazard

Certain lots of product have the potential for a sterile barrier breach.

Product Description & Identification

Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter

Affected Products

Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter

Additional Source Details

FieldValue
CityBrooklyn Park
StateMN
Event id98786
Address 17611 Northland Dr N
Code infoGTIN 00673978188447, Lot Numbers: 0231651336; GTIN 20643169454877, Lot Numbers: 0231651336, 0231651345, 0231651385, 0231651389, 0231651396, 0231667029, 0231667046, 0231757975, 0231758248, 0231758259, 0231936467, 0231982226, 0232274424, C232287618, C232287619, C232287620, C232598550, C232598552.
Postal code55428-1088
Report date20260527
Product typeDevices
Product quantity3790 units
Reason for recallCertain lots of product have the potential for a sterile barrier breach.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260421
Initial firm notificationLetter
Center classification date20260520

Overview

  • Recalling FirmMedtronic Perfusion Systems
  • StatusOngoing
  • Risk LevelClass II
  • 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, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.
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