FDA Device recall Z-1528-2016
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-1528-2016 |
| 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 | No Hole Shell 048mm Taper Size 2, Lot Codes: 322986, 323743, 320026, 322977, 323744; No Hole Shell 052mm Taper Size…No Hole Shell 048mm Taper Size 2, Lot Codes: 322986, 323743, 320026, 322977, 323744; No Hole Shell 052mm Taper Size 3, Lot Codes: 322396, 322971, 322403, 322984, 322985, 323750. |
|---|
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-1528-2016%22
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