FDA Device recall Z-2424-2016
O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants
- FDA Device
- Class II
- terminated
- Published 2016-08-24
On 2016-08-24 the FDA classified a Class II recall of O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 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-2424-2016 |
| 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
O-Ring Abutment 4.1mm(D) x 2mm(H) Item: OSO20 Dental implants
Reason
Pouches may not have been sealed during packing.
Identifiers
| code_info | Lot # 1002024, 1014103, 1022623, 1030863, 1031271, 1051924, 1054014, 1057816, 1068294, 1069738, 1071756, 1078857, 10823…Lot # 1002024, 1014103, 1022623, 1030863, 1031271, 1051924, 1054014, 1057816, 1068294, 1069738, 1071756, 1078857, 1082342, 1095159, 1095387, 1129684, 1131304, 1141288, 1161312, 1168381, 1169242, 1169931, 1170162, 1173357, 987787, and 987884 |
|---|
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-2424-2016%22
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