Sierra Scientific Instruments

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “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.
  • Source
    DH
  • 1 Event

One device in the database

  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Sierra Scientific Instruments ManoShield™ AR

One manufacturer with a similar name

Learn more about the data here

  • Manufacturer Address
    Sierra Scientific Instruments Inc, 5757 W Century Blvd Ste 660, Los Angeles CA 90045-6456
  • Source
    USFDA