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Catalog Number J2C1711 |
Device Problem
No Flow (2991)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 07/28/2023 |
Event Type
malfunction
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Manufacturer Narrative
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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 a small volume infusor would not flow.Two days after medication started, the patient visited the hospital to remove the device and the nurse observed no flow from the huber needle (not baxter product).The nurse removed the huber needle and confirmed no flow from the device luer adapter.There was no report of patient injury or medical intervention associated with this event.No additional information is available.
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Manufacturer Narrative
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H4: the lot was manufactured from december 07, 2022 to december 08, 2022.H10: the device was received for evaluation.A visual inspection did not identify any abnormalities that could have contributed to the reported condition.A functional flow rate test was performed, and the flow rates were found to be within the product specification range.The reported condition was not verified.The sample was determined to be a conforming product.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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