Sat 15 Aug 2026
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| Title | Date | File |
|---|---|---|
| (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 | ||
| (SG-1802-03-H) Urgent FSN of LIFEPAK 20e Defibrillator Manufactured by Physio-Control | ||
| (WU186), NCMDR Weekly Update | ||
| (SG-1802-02-H) Field Safety Notice-recall of Various Vital-Port Vascular Access Systems manufactured by Cook Medical | ||
| (WU185), NCMDR Weekly Update |
Last update date: 09/08/2026 at 11:41 AM Saudi Arabia time
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