Catalog Number 103530 |
Device Problem
Leak/Splash (1354)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/23/2021 |
Event Type
malfunction
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Manufacturer Narrative
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The device has been received and the evaluation is in progress.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 during treatment with a polyflux 140 h dialyzer, an external fluid leak occurred and an ungluing was observed at the header.There was no patient injury or medical intervention associated with this event.No additional information is available.
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Manufacturer Narrative
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H10: the device was received for evaluation.The visual inspection by naked eye showed the product wet.A leak test of the dialysate side was performed and a leak was observed.The cause were two cracks in the welding zone.The reported condition was verified.The cause of the crack 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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