B
Bob Bates
Dear Lorraine;
Thanks for the speedy reply. In my research today I came across something about the Medtronic Mosaic which gave me pause. It was not dated, so it could be very old data.
It was on :www.mdiconsultants.com/section_NI/FDA_Recalls/recallarchiev6.htm
It referenced a product recall for the Medronic Mosaic Porcine Bioprosthesis, for Aortic Valves, model numbers 30519,30521,30523,30535,30527. recall #Z-867/868-0.
Reason: " A misinterpretation in measurement of coaptation depth by a technician resulted in the release of out of specification devices."
I am guessing this issue has long been resolved, but its the first I heard about this, and thought it worth passing on.
Regards,
Bob
Thanks for the speedy reply. In my research today I came across something about the Medtronic Mosaic which gave me pause. It was not dated, so it could be very old data.
It was on :www.mdiconsultants.com/section_NI/FDA_Recalls/recallarchiev6.htm
It referenced a product recall for the Medronic Mosaic Porcine Bioprosthesis, for Aortic Valves, model numbers 30519,30521,30523,30535,30527. recall #Z-867/868-0.
Reason: " A misinterpretation in measurement of coaptation depth by a technician resulted in the release of out of specification devices."
I am guessing this issue has long been resolved, but its the first I heard about this, and thought it worth passing on.
Regards,
Bob