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 |
|---|---|---|
| Risk of occlusion of the airway when using Solus airway tube manufactured by Intersurgical Ltd. | 2017-06-15 |
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| (WU1724), NCMDR Weekly Update | 2017-06-13 |
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| Recall of Laser photocoagulator Easyret manufactured by Quantel Medical | 2017-06-08 |
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| (WU1723), NCMDR Weekly Update | 2017-06-06 |
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| (WU1722), NCMDR Weekly Update | 2017-05-29 |
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| (WU1721), NCMDR Weekly Update | 2017-05-23 |
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| (WU1720), NCMDR Weekly Update | 2017-05-16 |
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| (WU1719), NCMDR Weekly Update | 2017-05-08 |
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| (WU1718), NCMDR Weekly Update | 2017-05-02 |
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| Recall of a synthetic bone substitute manufactured by Kasios | 2017-05-02 |
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