Waldemar Link recalls a specific knee prosthesis segment due to potential failure to meet specifications. Affected units include the LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right with Item No. 15-2979/01.
The firm discovered through customer complaints that device segments may not meet specifications.
Waldemar Link is recalling a specific knee prosthesis segment that may not meet specifications. This could lead to improper function or complications after implantation. Patients using this segment should contact the manufacturer for details.
The prosthesis segment may not meet specifications, which could lead to improper function or complications after implantation. This issue arises from potential manufacturing inconsistencies that affect the segment's fit and performance.
Patients who have received the LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right with Item No. 15-2979/01 are affected. Those with this specific prosthesis segment are at risk of improper function.
Check for the product name: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right. Look for the item number 15-2979/01 and UDI-DI code 04026575328093.
Reach out to Waldemar Link directly to confirm if your prosthesis segment is affected and get instructions.
This recall specifically affects the LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right with Item No. 15-2979/01. Check your product details to see if you are affected.
Contact Waldemar Link directly to confirm if your segment is affected and get instructions on next steps.
Look for the product name: LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right, and check the item number 15-2979/01 or UDI-DI code 04026575328093.
We’ve drafted a message you can send Waldemar Link to request your refund or repair — edit it as you like.
Subject: Recall Z-2048-2023 — Waldemar Link Waldemar Link Hello, I own a Waldemar Link that is covered by recall Z-2048-2023 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.
