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Catalog Number UNKNOWN |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Unspecified Infection (1930)
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Event Date 08/26/2009 |
Event Type
Injury
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Manufacturer Narrative
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Internal complaint reference: (b)(4).Tan, p.W., ho, w.C., & song, c.(2009).The use of urgotul¿ in the treatment of partial thickness burns and split-thickness skin graft donor sites: a prospective control study.International wound journal, 6(4), 295-300.Doi: 10.1111/j.1742-481x.2009.00611.X.
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Event Description
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It was reported that on literature review "the use of in the treatment of partial thickness burns and split-thickness skin graft donor sites: a prospective control study", (2) patients developed a superficial infection after promote healing for burns and skin graft donor sites during the use of tulle-grass (tg) dressing (jelonet).The events were with antimicrobial therapy.Patients outcome is unknown.No further information is available.
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Manufacturer Narrative
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H3, h6: it was reported that on literature review "the use of in the treatment of partial thickness burns and split-thickness skin graft donor sites: a prospective control study", (2) patients developed a superficial infection after promote healing for burns and skin graft donor sites during the use of tulle-grass (tg) dressing (jelonet).The events were with antimicrobial therapy.Patients outcome is unknown.No further information is available.The device was not returned for analysis.We have therefore not been able to confirm a relationship between the event and the device, or identify a definitive root cause.A lot number for the device was not provided, therefore it was not possible to carry out a device history review.A complaint history review for the product family revealed a small number of similar instances in the last 12 months.A clinical evaluation was conducted.As no clinical information has been received (despite being requested), no clinical factors could be concluded to have contributed to the event(s).Furthermore, patient outcome(s) could not be determined.No further assessment was possible based on the information currently available.A risk management review was conducted and which mitigated the reported issue with no further action or updates required.As the specific device involved has not been identified within the complaint detail, a targeted review of labeling/product ifu cannot be carried out.A review concluded that there are no prior escalated actions related to this product and the reported event.A probable root cause for this complaint cannot be determined; there is no definitive link between the device and the adverse event.Possible causes could be that the dressing was not appropriate for the wound, that it was applied incorrectly or that there was inadequate preparation of the wound site before application.No further actions by smith & nephew are deemed necessary at this stage.However, we will continue to monitor for any adverse trends relating to this product range.Smith & nephew acknowledge customer concern and are continually investigating ways to develop and improve our products.
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Search Alerts/Recalls
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