FDA Device recall Z-2048-2023
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right
- FDA Device
- Class II
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class II recall of LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right by Waldemar Link And Kg Mfg Site, citing the firm discovered through customer complaints that device segments may not meet specifications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2048-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-03-18 |
| Published | 2023-07-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Waldemar Link And Kg Mfg Site |
| Distribution | AL, GA, IL, IN, KS, NJ, NY, TX |
Product
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right
Reason
The firm discovered through customer complaints that device segments may not meet specifications.
Identifiers
| code_info | Item No. 15-2979/01; UDI-DI: 04026575328093. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2048-2023%22
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