Weekly reports of the National Center for Medical Devices and Products Reporting
Weekly reports of the National Center for Medical Devices and Products Reporting
For more information, please visit the National Center for Medical Devices and Products Reporting Click Here
| Title | Date | File |
|---|---|---|
| (SG-1802-04-H) Urgent Recall of (Mesh Products) Restorelle DirectFix Manufactured by Coloplast | 2018-02-08 |
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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 | 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 |
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| (WU185), NCMDR Weekly Update | 2018-01-30 |
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| (WU184), NCMDR Weekly Update | 2018-01-23 |
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| (SG-1801-01-H) Update - Urgent FSN of Absorb and Absorb GT1 (BVS) Systems manufactured by Abbott with list | 2018-01-21 |
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| (WU182), NCMDR Weekly Update | 2018-01-16 |
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| (WU183), NCMDR Weekly Update | 2018-01-16 |
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