العنوان | التاريخ | ملف التحميل |
---|---|---|
(SG-1803-07-H) Urgent Safety notice of Fabius devices Manufactured by Draeger Medical Systems Inc | 2018-03-19 | |
(SG-1803-08-H)FSNs-Recalls issued by Zimmer need action | 2018-03-19 | |
(WU1811), NCMDR Weekly Update | 2018-03-13 | |
(WU1810), NCMDR Weekly Update | 2018-03-06 | |
(WU189), NCMDR Weekly Update | 2018-02-27 | |
(SG-1802-06-H) Urgent Recall of Mac Pin Non-Cannulated Screw Manufactured by Amendia, Inc (is now Spinal Elements, Inc.) | 2018-02-27 | |
(WU188), NCMDR Weekly Update | 2018-02-20 | |
(WU187), NCMDR Weekly Update | 2018-02-14 | |
(SG-1802-04-H) Urgent Recall of (Mesh Products) Restorelle DirectFix Manufactured by Coloplast | 2018-02-08 | |
(SG-1802-05-H) Urgent Recall of (Mesh Products) Uphold LITE with Capio SLIM and Solyx Single Incision Sling System Manufactured by Boston Scientific | 2018-02-08 |