Model Number 35303 |
Device Problem
Component Missing (2306)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 09/23/2021 |
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 one of the male external catheters were incorrectly packaged and the adhesive was on the packaging.Also stated that there was no direction for the items.The complainant stated that one catheter of 32 mm was remaining, and they would try it.The representative sent a link for an instruction video on male external catheters.It was noted that the patient had been using the product for less than 90 days.
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Event Description
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It was reported that one of the male external catheters were incorrectly packaged and the adhesive was on the packaging.Also stated that there was no direction for the items.The complainant stated that one catheter of 32 mm was remaining, and they would try it.The representative sent a link for an instruction video on male external catheters.It was noted that the patient had been using the product for less than 90 days.Per customer contact via phone on 11nov2021, it was stated that there were no directions on how to use the male external catheters and there was no measurement tool.As a new user, they needed this and it was later stated that they were offered a link to a video that explained things.Per follow-up via phone on 17nov2021 , customer stated about the sizing guide used for measuring the penis when ordering condom catheters but patient did not have a sizing guide.
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Manufacturer Narrative
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The reported event was inconclusive because no sample was returned.A potential root cause for this failure could be "placement omission".It was unknown whether the device had met specifications.Based on patient code 2645 the product does not appear to have been used.However, the product is intended to be used for treatment purpose but it is unknown whether the product had a relationship with the reported event.The device was not returned for evaluation.The lot number is unknown; therefore, the device history record could not be reviewed.A labeling review was not performed because labeling could not have prevented the reported failure.The device was not returned.
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Search Alerts/Recalls
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