Home › Device types › PAX
Surgical Kit
FDA product code PAX · Class f · Unknown
1
Registered devices
0
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-27 | Alcon Research, Ltd. | Alcon is initiating a Voluntary Medical Device Removal because the product supplier has stated that there is potential for sterile packaging to be compromised. |
| 2016-11-09 | Elana, Inc. | Elana has issued this Field Action to voluntarily remove specific serial numbers of our Elana Surgical KitHUD due to potentially compromised integrity of the ou |
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