Catalog Number 7N8301 |
Device Problems
Tear, Rip or Hole in Device Packaging (2385); Difficult to Open or Remove Packaging Material (2922)
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Patient Problem
No Patient Involvement (2645)
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Event Date 12/21/2020 |
Event Type
malfunction
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Manufacturer Narrative
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The device was received and is currently awaiting evaluation completion.Should additional relevant information become available, a supplemental report will be submitted.
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Event Description
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It was reported that the sterile packaging of one-link non-dehp standard bore catheter extension set was tearing and would not open correctly.This was identified prior to use.There was no patient involvement.No additional information is available.
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Manufacturer Narrative
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H10: the device was received for evaluation.Visual inspection was performed which observed that the sterile packaging was damaged (tear).The reported condition was verified.The cause of the condition could not be determined.A batch review was conducted and there were no deviations found related to this reported condition during the manufacture of this lot.Should additional relevant information become available, a supplemental report will be submitted.
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Search Alerts/Recalls
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