LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
Reported: July 5, 2023 Initiated: March 18, 2021 #Z-2047-2023
Product Description
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
Reason for Recall
The firm discovered through customer complaints that device segments may not meet specifications.
Details
- Recalling Firm
- Waldemar Link GmbH & Co. KG (Mfg Site)
- Units Affected
- 22 units
- 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.
- Location
- Norderstedt, N/A
Frequently Asked Questions
What product was recalled? ▼
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left. Recalled by Waldemar Link GmbH & Co. KG (Mfg Site). Units affected: 22 units.
Why was this product recalled? ▼
The firm discovered through customer complaints that device segments may not meet specifications.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 5, 2023. Severity: Moderate. Recall number: Z-2047-2023.
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