Reported Jul 5, 2023 · Ongoing
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
Waldemar Link GmbH & Co. KG (Mfg Site)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Waldemar Link GmbH & Co. KG (Mfg Site) · Oststr. 4-10 · Norderstedt, N/A · N/A
Is this the product you have?
- LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Left
- Lot codes and dates
- Item No. 15/2973/06
- UDI-DI04026575340736
- Amount recalled
- 22 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
The firm discovered through customer complaints that device segments may not meet specifications.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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