Medtronic Perfusion Systems recalls Octopus Evolution Tissue Stabilizer, Model TS2000
See all recalls from Medtronic Perfusion Systems →Recalled Product
Octopus Evolution Tissue Stabilizer, Model TS2000
Hazard / Issue
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.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 00643169668911; Serial Numbers: 0232992409 0233010063 0233010115
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Octopus Evolution Tissue Stabilizer, →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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