The sample device was indicated as available for evaluation.Argon has made three good faith efforts in requesting the return of the device, however, as of the date of this report the device has not yet been returned.Without such evidence, a root cause cannot be determined.If additional information is received in the future, the issue will be re-evaluated as needed.
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Picc was inserted on (b)(6) 2020 at 1600 with no complications.On (b)(6) 2020 at 1500 phlebitis was noted next to the insertion site.Warm compress was applied and the leg was elevated, md ordered to continue to assess the patients leg and monitor for improvement.On (b)(6) 2020 when md reassessed picc line, no improvement was seen, the redness was worse, cord could be felt along the picc line and near the insertion and the swelling was more significant.Md ordered the picc to be removed.The picc line was removed successfully, no leak noted after removal.
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