Octopus 4 Tissue Stabilizer, Model 29400
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 4 Tissue Stabilizer, Model 29400
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: 00763000543679UPC 00763000543679Would you have heard about this one?
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