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Sharps Needle Destruction Device
FDA product code MTV · Class 2 · General Hospital
0
Registered devices
2
Adverse events
1
Recalls
1
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2002-08-15 | E Med Future Inc | Their NeedleZap devices were not manufactured in accordance with the Quality System Regulations, and were shipped without an approved PMA. |
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