العنوان | التاريخ | ملف التحميل |
---|---|---|
(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 | |
(WU186), NCMDR Weekly Update | 2018-02-06 | |
(SG-1802-03-H) Urgent FSN of LIFEPAK 20e Defibrillator Manufactured by Physio-Control | 2018-02-06 | |
(SG-1802-02-H) Field Safety Notice-recall of Various Vital-Port Vascular Access Systems manufactured by Cook Medical | 2018-02-04 | |
(WU185), NCMDR Weekly Update | 2018-01-30 | |
(WU184), NCMDR Weekly Update | 2018-01-23 |