FDA Device recall Z-1526-2016
Trinity Acetabular System 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 System 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-1526-2016 |
| 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 System Product Usage - Total Hip Replacement.
Reason
Potential for abrasion of the sterile barrier pouches of the new packaging system.
Identifiers
| code_info | Non Occluded TPS Shell 048mm Taper SZ2, Lot Code: 323741 |
|---|
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-1526-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.