Wed 26 Aug 2026
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| Title | Date | File |
|---|---|---|
| (SG-1803-08-H)FSNs-Recalls issued by Zimmer need action | ||
| (SG-1803-07-H) Urgent Safety notice of Fabius devices Manufactured by Draeger Medical Systems Inc | ||
| (WU1811), NCMDR Weekly Update | ||
| (WU1810), NCMDR Weekly Update | ||
| (SG-1802-06-H) Urgent Recall of Mac Pin Non-Cannulated Screw Manufactured by Amendia, Inc (is now Spinal Elements, Inc.) | ||
| (WU189), NCMDR Weekly Update | ||
| (WU188), NCMDR Weekly Update | ||
| (WU187), NCMDR Weekly Update | ||
| (SG-1802-05-H) Urgent Recall of (Mesh Products) Uphold LITE with Capio SLIM and Solyx Single Incision Sling System Manufactured by Boston Scientific | ||
| (SG-1802-04-H) Urgent Recall of (Mesh Products) Restorelle DirectFix Manufactured by Coloplast |
Last update date: 31/08/2026 at 09:22 AM Saudi Arabia time
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