Davinci- what a scam

Discussion in 'Intuitive Surgical Patient Discussions' started by Anonymous, Jun 22, 2012 at 7:09 PM.

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  1. anonymous

    anonymous Guest

    P.S. (sidebar from my husband) you might want to think of diversifying in the near future! Moron.
     

  2. anonymous

    anonymous Guest

    Yes and at age 40, i have $890,000 of vested monies in my 401K. Planning to retire here when im 55.
     
  3. anonymous

    anonymous Guest

    Is that supposed to mean something to me?
     
  4. anonymous

    anonymous Guest

    You did well my friend.
     
  5. anonymous

    anonymous Guest

    I see that!! Wonderful because we really need someone in manufacturing who knows something about regulatory processes and procedures!! We are getting slammed with “nonconforming materials” and now we need to hire someone qualified for this role. Here is that posting you referenced on Indeed:

    Job: Regulatory and Quality
    Primary Location: United States-California-US-CA-Sunnyvale
    Schedule: Full-time
    Requisition ID: 180884

    Primary function of position:

    The Quality Assurance (QA) Associate is responsible for reviewing device history records (DHRs) for accuracy and completeness, certifying compliance to product specification and traceability requirements and ensuring that any deviations from the manufacturing process were properly recorded and authorized by members of the appropriate departments.

    Intuitive Surgical has identified they don’t have knowledgeable employees in this role.

    Per the FDA:
    Control of Nonconforming Product - 21 CFR 820.90(a)

    Determine if the manufacturer has established procedures to "control" nonconforming product. The procedure must "address the identification, documentation, evaluation, segregation, and disposition of nonconforming product." The procedure must also include a "determination of the need for an investigation." The evaluation and any investigation must be documented, including documented explanations for not performing an investigation. Documentation should also include how nonconformances will be trended and/or monitored.

    Fda showed 3 recalls this month alone!!!

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=164959

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=165193

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=165194

    Due to : Nonconforming Material/Component

    Really hopeful someone who knows the industry and has the right education and background is hired for this position this time around!!
     
  6. anonymous

    anonymous Guest

    They are getting filled fast and hardly any internal hires.
     
  7. anonymous

    anonymous Guest

    I am always amazed with the level of ignorance ISI has around anything they post.

    You do realize Any money you contribute from your paycheck is always 100% yours?? The small comparison % of your companies contribution and their vesting schedule is really insignificant as you aren’t even at 1m yet with what you claim is “vested.” Also the purpose of a 401k is to not put money into your own company as the one and only stock. 401ks are for safety in diversification!! Thus the reason it is called a “portfolio.”

    are you sure you are not talking about your ESPP (employee stock purchase plan) or your stock options? I just hate for you to keep looking so stupid, hun....
     
  8. anonymous

    anonymous Guest

    I see that!! Wonderful because we really need someone in manufacturing who knows something about regulatory processes and procedures!! We are getting slammed with “nonconforming materials” and now we need to hire someone qualified for this role. Here is that posting you referenced on Indeed:

    Job: Regulatory and Quality
    Primary Location: United States-California-US-CA-Sunnyvale
    Schedule: Full-time
    Requisition ID: 180884

    Primary function of position:

    The Quality Assurance (QA) Associate is responsible for reviewing device history records (DHRs) for accuracy and completeness, certifying compliance to product specification and traceability requirements and ensuring that any deviations from the manufacturing process were properly recorded and authorized by members of the appropriate departments.

    Intuitive Surgical has identified they don’t have knowledgeable employees in this role.

    Per the FDA:
    Control of Nonconforming Product - 21 CFR 820.90(a)

    Determine if the manufacturer has established procedures to "control" nonconforming product. The procedure must "address the identification, documentation, evaluation, segregation, and disposition of nonconforming product." The procedure must also include a "determination of the need for an investigation." The evaluation and any investigation must be documented, including documented explanations for not performing an investigation. Documentation should also include how nonconformances will be trended and/or monitored.

    Fda showed 3 recalls this month alone!!!

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=164959

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=165193

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=165194

    Due to : Nonconforming Material/Component

    Really hopeful someone who knows the industry and has the right education and background is hired for this position this time around!!
     
  9. anonymous

    anonymous Guest

    Because this cutting edge technology is sought after and the public is aware of the immense benefits of non invasive surgery. Its FDA approved and safer than traditional methods. Less recovery time for patients is the driving factor.
     
  10. anonymous

    anonymous Guest

    You probably want to increase the % you are contributing per paycheck. You said you are 40?? You are getting up there in age and close to retirement dude. I had that when I was 30 and it still wasn’t enough for a comfortable retirement plan. It might be okay now since my Da Vinci Surgery shaved a good decade off of my expected life span though...
     
  11. anonymous

    anonymous Guest

    All true. Thank God for DaVinci !!!
     
  12. anonymous

    anonymous Guest

    Answer my previous questions and I will show you. Dwas has spoon fed ISI through the history of this board with nothing but facts with supporting documentation. It is your turn.
     
  13. anonymous

    anonymous Guest

    To remind you, here is the list you are respond to:

    1) Patent Fraud - ISI reported a patent for their flexible robotics platform to their investors that was actually referencing a locomotive air flow feature from 1912.
    2) Product Liability \ Negligence - What are the plans to address the FDA reported "known defect" of the ESU's conductor wires.
    3) Product Liability \ Negligence - What is ISIs plan to reply to the FDA on their notice for using AEM in ESU's
    4) Product Liability \ Negligence - What was the root cause of the three deaths this month reported to the FDA
    5) Product Liability \ Negligence - Why are parts that were recalled 4 years ago appearing in operating rooms around the country?
     
  14. anonymous

    anonymous Guest

    ISI can’t answer your questions because they are riddled with direct responsibilities for intuitive Surgical to actually do something about the negligence, fraud, and liabilities. Too messy and the questions are too hard for us to answer. Just let us keep copying and pasting nonsense that diverts attention from our own corruption.
     
  15. anonymous

    anonymous Guest

    Thank you! Now reply with the answers

    1) Patent Fraud - ISI reported a patent for their flexible robotics platform to their investors that was actually referencing a locomotive air flow feature from 1912.
    2) Product Liability \ Negligence - What are the plans to address the FDA reported "known defect" of the ESU's conductor wires.
    3) Product Liability \ Negligence - What is ISIs plan to reply to the FDA on their notice for using AEM in ESU's
    4) Product Liability \ Negligence - What was the root cause of the three deaths this month reported to the FDA
    5) Product Liability \ Negligence - Why are parts that were recalled 4 years ago appearing in operating rooms around the country?
     
  16. anonymous

    anonymous Guest

    Siting sources for previous post:

    Supporting material documenting above statement accuracy:

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=7648276&pc=NAY

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/results.cfm

    https://www.fda.gov/ICECI/EnforcementActions/WarningLetters/ucm363260.htm

    http://www.cafepharma.com/boards/threads/davinci-what-a-scam.505456/page-1188
    (Copies of legal documents showing no AEM but isi caught in another lie of KNOWING they need to incorporate it)

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/detail.cfm?mdrfoi__id=7582936&pc=NAY
    (One of many single site cannula recalls showing up in operating rooms 4 years later)

    https://patents.justia.com/assignee/intuitive-surgical
    (New robot design patents)
     
  17. anonymous

    anonymous Guest

    Its hilarious, but also sad and pathetic you have to answer your own posts.
    TEAM ISI # 1
     
  18. anonymous

    anonymous Guest

    Even it that was an accurate statement - not really any of those things...Now focus, little lemming, and answer the questions. No one cares about what you think is hilarious, sad or pathetic.
     
  19. anonymous

    anonymous Guest

    They've been doing it since 2012. Go back and see the madness and how deranged the DWAS shill is
     
  20. anonymous

    anonymous Guest

    ISRG is expected to report $2.50/share on $868M+ in revenue. The Streets whisper number is $2.65 which I'd lean towards. When earnings report comes out after closing bell next Thursday, ISRG will soar. Buy NOW!!