Model Number 479688 |
Device Problems
Premature Activation (1484); Activation, Positioning or Separation Problem (2906)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/25/2020 |
Event Type
malfunction
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that upon opening of the left ventricular (lv) lead from the sterile box, it was observed that the screw was out of the tip of the lead.The physician retracted the tip and decided to replace lead instead.No patient complications have been reported as a result of this event.
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Manufacturer Narrative
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If information is provided in the future, a supplemental report will be issued.
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Search Alerts/Recalls
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