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(WU1810), NCMDR Weekly Update
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(WU189), NCMDR Weekly Update
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(SG-1802-06-H) Urgent Recall of Mac Pin Non-Cannulated Screw Manufactured by Amendia, Inc (is now Spinal Elements, Inc.)
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(WU188), NCMDR Weekly Update
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(WU187), NCMDR Weekly Update
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(SG-1802-04-H) Urgent Recall of (Mesh Products) Restorelle DirectFix Manufactured by Coloplast
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(SG-1802-05-H) Urgent Recall of (Mesh Products) Uphold LITE with Capio SLIM and Solyx Single Incision Sling System Manufactured by Boston Scientific
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(WU186), NCMDR Weekly Update
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(SG-1802-03-H) Urgent FSN of LIFEPAK 20e Defibrillator Manufactured by Physio-Control
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(SG-1802-02-H) Field Safety Notice-recall of Various Vital-Port Vascular Access Systems manufactured by Cook Medical
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