Waldemar Link recalls left knee prosthesis size 4 (Item No. 15-2979/02) due to potential manufacturing defects that may not meet specifications. Affected patients should contact the company for details.
The firm discovered through customer complaints that device segments may not meet specifications.
Waldemar Link is recalling left knee prosthesis segments size 4 for possible manufacturing defects that might not meet specifications. This could affect the safety and proper function of the prosthesis.
The prosthesis segment may not meet specifications, which could lead to improper function or safety issues during use. This defect might not cause immediate harm but could affect the prosthesis's performance.
Patients who received the LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left (Item No. 15-2979/02) are affected. Those with this specific prosthesis segment are at risk of potential improper function.
Check for the product name 'LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left' with item number 15-2979/02. The UDI-DI code 04026575328109 is also associated with this product.
Reach out to Waldemar Link for specific instructions on whether the prosthesis segment needs to be replaced or adjusted.
This recall specifically affects the LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left with item number 15-2979/02. Check your product details to see if you are affected.
Contact Waldemar Link directly for guidance on whether your prosthesis needs replacement or adjustment.
The recall states the segments may not meet specifications, but no specific risk of serious injury is mentioned. The hazard is described as a potential issue with function, not immediate safety risks.
We’ve drafted a message you can send Waldemar Link to request your refund or repair — edit it as you like.
Subject: Recall Z-2049-2023 — Waldemar Link Waldemar Link Hello, I own a Waldemar Link that is covered by recall Z-2049-2023 from Waldemar Link. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
