Medtronic TurboHawk Catheter Recall Issued Due to Tips Breaking
The FDA has given a class I designation to a recall of Medtronic TurboHawk atherectomy systems due to a risk of the catheter tips breaking off and causing life-threatening arterial…
The FDA has given a class I designation to a recall of Medtronic TurboHawk atherectomy systems due to a risk of the catheter tips breaking off and causing life-threatening arterial…
A Tasigna lawsuit filed by a North Carolina woman claims the leukemia drug's side effects resulted in a partial leg amputation.