Octopus Evolution Tissue Stabilizer, Model TS2000
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 Tissue Stabilizer, Model TS2000
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: 00643169668911Model Serial Numbers: 0232992409 0233010063 0233010115UPC 00643169668911Would you have heard about this one?
RapidRecall watches everything you own against every new federal recall and emails you the moment something you bought turns up. Free for your most important items.
Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.