Device Problems
Inaccurate Flow Rate (1249); No Flow (2991)
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Patient Problems
No Consequences Or Impact To Patient (2199); Injury (2348)
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Event Type
malfunction
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Manufacturer Narrative
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The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.The device was not returned.
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Event Description
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It was reported that the silicone coude foley catheter that was inserted pre-op initially drained some urine, however there was no urine output after a significant amount of iv fluids were given to the patient.After surgery, the nurse and physician were unable to deflate the balloon to get the catheter out of the patient.The catheter was then surgically removed from the patient and the patient allegedly experienced bulbar urethral trauma related to the coude tip foley catheter.
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Manufacturer Narrative
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The device was not returned for evaluation.The lot number is unknown; therefore, a device history record could not be reviewed.Although the product family is unknown, the all silicone catheter ifus are found to be adequate based on past reviews.
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Event Description
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It was reported that the silicone coude foley catheter that was inserted pre-op initially drained some urine, however there was no urine output after a significant amount of iv fluids were given to the patient.After surgery, the nurse and physician were unable to deflate the balloon to get the catheter out of the patient.The catheter was then surgically removed from the patient and the patient allegedly experienced bulbar urethral trauma related to the coude tip foley catheter.
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Search Alerts/Recalls
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