“If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
Part Numbers:
- 9733449 Straight Suction EM, ENT
- 9733450 Curved Suction 70, EM
- 9733451 Short Curved Suction 90, EM
- 9734308 Suction Small AxiEMTM ENT
See Attached FSN for full list