FDA Device recall Z-1527-2016
Trinity Acetabular Shell Product Usage: Total Hip Replacement
- FDA Device
- Class II
- terminated
- Published 2016-05-04
On 2016-05-04 the FDA classified a Class II recall of Trinity Acetabular Shell Product Usage: Total Hip Replacement by Corin Usa, citing potential for abrasion of the sterile barrier pouches of the new packaging system.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1527-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-01-29 |
| Published | 2016-05-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Corin Usa |
| Distribution | US |
Product
Trinity Acetabular Shell Product Usage: Total Hip Replacement.
Reason
Potential for abrasion of the sterile barrier pouches of the new packaging system.
Identifiers
| code_info | Cluster Shell 044mm Taper Size 1, Lot Code: 320023; Cluster Shell 046mm Pager Size 2, Lot Code: 320018; Cluster Shell…Cluster Shell 044mm Taper Size 1, Lot Code: 320023; Cluster Shell 046mm Pager Size 2, Lot Code: 320018; Cluster Shell 048mm Taper Size 2, Lot Codes: 321691, 322402, 322981, 322982, 323745, 323746, 324298; Cluster Shell 050mm Taper Size 2, Lot Codes: 321954, 322753, 322980; Cluster Shell 050mm Taper Size 3, Lot Codes: |
|---|
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-1527-2016%22
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