(b)(4).To date the device has not been returned.If the device or further details are received at a later date a supplemental medwatch will be sent.Attempts are being made to obtain the following information.To date no response has been provided.If further details are received at a later date a supplemental medwatch will be sent.Were the cases discussed in this article previously reported to ethicon? if yes, please provide a complaint reference number.Does the surgeon believe that ethicon sutures involved caused and/or contributed to the post-operative complications described in the article? does the surgeon believe there was any deficiency with the ethicon sutures used in this procedure? are the product code and lot numbers available for all ethicon devices used? citation: clinical neurology and neurosurgery 125 (2014) 137¿142.Http://dx.Doi.Org/10.1016/j.Clineuro.2014.07.026.
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