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 |
|---|---|---|
| (WU1747), NCMDR Weekly Update | 2017-11-21 |
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| Recall of FlexCath Advance Steerable Sheath manufactured by Medtronic | 2017-11-20 |
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| (WU1746), NCMDR Weekly Update | 2017-11-14 |
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| Recall of DORO Sterile Disposable Skull Pins | 2017-11-13 |
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| (WU1745), NCMDR Weekly Update | 2017-11-07 |
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| Recall of foldable Intraocular lenses , Lentis | 2017-11-05 |
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| (WU1744), NCMDR Weekly Update | 2017-10-30 |
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| (WU1743), NCMDR Weekly Update | 2017-10-24 |
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| (WU1742), NCMDR Weekly Update | 2017-10-17 |
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| (Malfunction in Intra-Aortic Balloon Pumps (IABP) manufactured by Maquet | 2017-10-15 |
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