Medtronic Recalls Octopus Nuvo Tissue Stabilizer Over Potential Fracturing of Surgical Device Component That Could Potentially Cause Heart Tissue Damage.
A class I surgical device recall has been issued by Medtronic, Inc. (Medtronic”) recalling approximately 571 Medtronic Octopus Nuvo Tissue Stabilizers distributed to healthcare facilities reportedly because a component of the Medtronic Octopus Nuvo Tissue Stabilizer medical device could fracture during use and fragments of the component could potentially fall into the patient’s chest cavity and/or damage the heart tissue, according to a Food & Drug Administration (“FDA”) medical device recall news report.
For more information on the Medtronic Octopus Nuvo Tissue Stabilizer surgical device recall, call Medtronic at 1‐877‐526‐7890.
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