Medtronic Perfusion Systems Recalls
12 recalls on record in the United States
Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone
Certain lots of product have the potential for a sterile barrier breach.
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Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silic
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicon
Certain lots of product have the potential for a sterile barrier breach.
View recall details →
Medtronic Perfusion Systems recalls Octopus Evolution AS Tissue Stabilizer, Model TS2500
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, and the long tube was attached to the top, contrary to the intended design.
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Medtronic Perfusion Systems recalls Octopus 4 Tissue Stabilizer, Model 29400
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, and the long tube was attached to the top, contrary to the intended design.
View recall details →
Medtronic Perfusion Systems recalls Octopus Evolution Tissue Stabilizer, Model TS2000
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, and the long tube was attached to the top, contrary to the intended design.
View recall details →