FDA Device recall Z-2517-2016
Certain EP Healing 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 EP Healing 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-2517-2016 |
| 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 EP Healing Abutment Dental implants
Reason
Pouches may not have been sealed during packing.
Identifiers
| code_info | Items: IMHA352, IMHA353, IMHA356, ITHA58, ITHA63, ITHA64, ITHA66. ITHA68, ITHA73, ITHA74, ITHA76, ITHA78, IWTH52, IWTH…Items: IMHA352, IMHA353, IMHA356, ITHA58, ITHA63, ITHA64, ITHA66. ITHA68, ITHA73, ITHA74, ITHA76, ITHA78, IWTH52, IWTH54, IWTH56, IWTH58, IWTH562, IWTH564, IWTH566, IWTH568, IWTH572, IWTH573, IWTH574, IWTH576, IWTH578, IWTH62, IWTH63, IWTH64, IWTH66, IWTH68, IWTH672, IWTH673, IWTH674, IWTH676 AND IWTH678. |
|---|
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-2517-2016%22
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