Drug recall
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
FDA recall event 92500 · Class II · Waldemar Link GmbH & Co. KG (Mfg Site)
Key facts
| Event ID | 92500 |
|---|---|
| Recall numbers | Z-2046-2023, Z-2047-2023, Z-2048-2023, Z-2049-2023 |
| Recalling firm | Waldemar Link GmbH & Co. KG (Mfg Site) |
| Product type | Devices |
| Products | LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left, LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right, LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left, LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The firm discovered through customer complaints that device segments may not meet specifications. |
| Initiation date | Mar 18, 2021 |
| Report date | Jul 5, 2023 |
| City | Norderstedt |
| Country | Germany |
| FEI number | 3003386935 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: