(b)(4).(b)(4) has just received the incident device and has been assigned to engineering for evaluation.A follow-up report will be sent upon completion of investigation.In accordance to 21 cfr 803.56, if we obtain additional information, which was not known or was not available when the initial report was submitted, then the supplemental report will be submitted to the fda.
|
Investigation summary: one (1) event unit was returned for evaluation.Engineering was unable to test the unit for functionality due to the severity of the bent shaft.The unit was disassembled and all internal components met specifications.On march 18, 2016, applied medical issued a voluntary recall of the ca090 direct drive® clip applier due to increased customer feedback indicating inconsistent clip application.Although malformed clips are typically readily apparent to the user, this failure mode may lead to unoccluded vessels.We regret this disruption in supply, yet believe that this is in the best interest of our customers.Additional information was requested and provided.In accordance to 21 cfr 803.56, if we obtain additional information, which was not known or was not available when this report was submitted, then a supplemental report will be submitted to the fda.
|