# FDA recall Z-2049-2023

> **Waldemar Link GmbH & Co. KG (Mfg Site)** · Class II · device recall initiated 2021-03-18.

## Product

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left

## Reason for recall

The firm discovered through customer complaints that device segments may not meet specifications.

## Distribution

Domestic: AL, GA, IL, IN, KS, NJ, NY, and TX. Foreign: Argentina, Australia, Austria, Brazil, Finland, France, Germany, India, Italy, Spain, and United Kingdom.

## Key facts

- **Recall number:** Z-2049-2023
- **Recalling firm:** Waldemar Link GmbH & Co. KG (Mfg Site)
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-03-18
- **Report date:** 2023-07-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Norderstedt, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2049-2023

## Citation

> AI Analytics. FDA recall Z-2049-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2049-2023. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*