FDA Device recall Z-2494-2016
Certain Provide Abutment Dental implants
- FDA Device
- Class II
- terminated
- Published 2016-08-24
On 2016-08-24 the FDA classified a Class II recall of Certain Provide Abutment Dental implants by Biomet 3i, citing pouches may not have been sealed during packing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2494-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-11-25 |
| Published | 2016-08-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Biomet 3i |
| Distribution | US |
Product
Certain Provide Abutment Dental implants
Reason
Pouches may not have been sealed during packing.
Identifiers
| code_info | Items: IPA4140, IPA4155, IPA4240, IPA4255, IPA4340, IPA4355, IPA4440, IPA4455, IPA5140, IPA5155, IPA5240, IPA5255, IPA…Items: IPA4140, IPA4155, IPA4240, IPA4255, IPA4340, IPA4355, IPA4440, IPA4455, IPA5140, IPA5155, IPA5240, IPA5255, IPA5340, IPA5355, IPA5440, IPA5455, IPA6140, IPA6155, IPA6240, IPA6255, IPA6340, IPA6355, IPA6440 and IPA6455. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2494-2016%22
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