Catalog Number 171305-000140 |
Device Problem
Fluid/Blood Leak (1250)
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Patient Problem
No Information (3190)
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Event Date 12/14/2018 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).The device has not been returned for investigation.Teleflex will continue to monitor and trend related events.
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Event Description
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Customer reported that "on 14 and 15 december one patient received on the emergency (b)(6) a bladder catheter.These catheters came out with a broken balloon in both cases.On the 15.12.Patient received the same bladder catheter again in the evening at our station.This one slipped also out of patient again on 16.12.In the morning, because the balloon was broken again.I talked to the nf and they used the same catheters with the same batch number: 171305.Of course, we are aware that the problem could be related to the patient's bladder.We report it as a precaution, because there might also be a material problem.
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Manufacturer Narrative
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(b)(4).The device lot number was not provided; therefore a ohr review could not be conducted.No sample was returned for investigation; therefore, no physical investigation could be conducted.Leak balloon could be due to several reasons.However, in the absence of returned sample and limited information available on this complaint , further investigation could not be conducted and therefore complaint is not confirmed.
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Event Description
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Customer reported that "on 14 and 15 december one patient received on the emergency sonnenhof a bladder catheter.These catheters came out with a broken balloon in both cases.On the 15.12.Patient received the same bladder catheter again in the evening at our station.This one slipped also out of patient again on 16.12.In the morning, because the balloon was broken again.I talked to the nf and they used the same catheters with the same batch number: 171305.Of course, we are aware that the problem could be related to the patient's bladder.We report it as a precaution, because there might also be a material problem.
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Search Alerts/Recalls
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