Device Problems
Use of Device Problem (1670); Improper or Incorrect Procedure or Method (2017)
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Patient Problems
Patient Problem/Medical Problem (2688); No Code Available (3191)
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Event Date 05/01/2016 |
Event Type
Injury
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Manufacturer Narrative
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Prepex is sold and used in (b)(6), it is neither sold nor used in the usa.Receiving reports regarding aes is very challenging and the company makes every effort to gain as much information as possible.The company did not begin reporting any aes to the fda until it was demanded by the fda.As a result there is a gap between the time of the ae and the reporting.This issue will resolve itself during 2017 when the company will report to the fda as required and requested.
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Event Description
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Improper placement led to incomplete foreskin removal patient referred to surgical correction.
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Manufacturer Narrative
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Prepex is sold and used in (b)(6), it is neither sold nor used in the usa.Receiving reports regarding aes is very challenging and the company makes every effort to gain as much information as possible.The company did not begin reporting any aes to the fda until it was demanded by the fda.As a result there is a gap between the time of the ae and the reporting.This issue will resolve itself during 2017 when the company will report to the fda as required and requested.No manufacturer investigation was undertaken since this was a foreseen risk in device usage and is clearly noted both in the ifu and the training program.Device unavailable.
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Event Description
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Improper placement led to incomplete foreskin removal patient referred to surgical correction.
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Search Alerts/Recalls
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