Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right
Brand
Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany
Lot Codes / Batch Numbers
Item No. 15-2973/05, UDI-DI: 04026575340699.
Products Sold
Item No. 15-2973/05; UDI-DI: 04026575340699.
Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany is recalling LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right due to The firm discovered through customer complaints that device segments may not meet specifications.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm discovered through customer complaints that device segments may not meet specifications.
Recommended Action
Per FDA guidance
The firm sent recall notifications by email to consignees on 03/24/2021. Customers were asked to discontinue use of affected devices and to return any that remain in stock to LinkBio Corporation, Waldemar Link's US Distributor, immediately. Credit or replacement was issued for the returned product upon receipt. Any questions about this recall event are to be directed to Nikhil Mangale at 1-973-625-1333 ext. 116 from Monday through Friday from 8:00 am to 5:30 pm, or by email to n.mangale@linkbio.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, GA, IL, IN, KS, NJ, NY, TX
Page updated: Jan 10, 2026