Octopus Evolution AS Tissue Stabilizer, Model TS2500
Medtronic Perfusion Systems
The hazard
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. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Octopus Evolution AS Tissue Stabilizer, Model TS2500
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model UDI-DI: 00643169668904Model 00613994764379UPC 00643169668904UPC 00613994764379Would you have heard about this one?
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