Lot Recall for the S.M.A.R.T. ® Nitinol Stent System and S.M.A.R.T. ® CONTROL ® Nitinol Stent System, Cordis
2012.08.22
Product group Non-active implants - special implants
Reference 02503/12
The manufacturer Cordis is conducting a recall for certain lot numbers of the S.M.A.R.T. ® Nitinol Stent System and the S.M.A.R.T. ® CONTROL ® Nitinol Stent System. Reason for the recall is a potential sterility breach due to holes or tears in the Tyvek ® side of the packaging.