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Model Number LF1937 |
Device Problems
Mechanical Problem (1384); Difficult to Open or Close (2921)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/05/2024 |
Event Type
malfunction
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Manufacturer Narrative
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Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
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Event Description
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According to the reporter, during a procedure, device could not be disconnected at all. the blade of the scalpel did not advance.Although the handle was able to be squeezed, unable to pull the trigger of the knife and was having difficulty releasing the handle.There was no patient injury.
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Search Alerts/Recalls
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