FDA Device recall Z-1694-2021
Logical cup liner - Product Usage: intended to replace a hip joint where bone stock is sufficient to support the implant
- FDA Device
- Class II
- terminated
- Published 2021-06-09
On 2021-06-09 the FDA classified a Class II recall of Logical cup liner - Product Usage: intended to replace a hip joint where bone stock is sufficient to support the implant by Signature Orthopedics, citing product mislabeled, with the incorrect product inside the package.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1694-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-04-20 |
| Published | 2021-06-09 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Signature Orthopedics |
| Distribution | US |
Product
Logical cup liner - Product Usage: intended to replace a hip joint where bone stock is sufficient to support the implant.
Reason
Product mislabeled, with the incorrect product inside the package.
Identifiers
| code_info | LOT# 71541-1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1694-2021%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.