Waldemar Link recalls Endo-Model SL Connection Components with serial numbers 250513/2083-2108 and 251013/3245-3254 due to potential screw shaft fracture causing bushing detachment. Affected users should contact the manufacturer for details.
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
Waldemar Link is recalling Endo-Model SL Connection Components with specific serial numbers because a screw shaft fracture could cause the bushing to detach. This poses a risk of serious injury during medical procedures.
The component's plateau screw may fracture longitudinally, causing the bushing to detach from the screw shaft. This could lead to complications during medical procedures if the implant becomes unstable.
Medical professionals using the Endo-Model SL Connection Components for surgical implants are most at risk. Patients who have received these components should contact their healthcare provider.
Check the serial numbers listed: 250513/2083 through 251105/0040. The product includes a PE-Plateau and is sold under item number 16-2840/05.
Reach out to Waldemar Link for specific instructions on how to handle the recalled components.
The plateau screw may fracture, causing the bushing to detach from the screw shaft, which could lead to serious complications during medical procedures.
Check the serial numbers listed: 250513/2083 through 251105/0040. The product includes a PE-Plateau and is sold under item number 16-2840/05.
Contact Waldemar Link for specific instructions on how to handle the recalled components.
We’ve drafted a message you can send Waldemar Link to request your refund or repair — edit it as you like.
Subject: Recall Z-1511-2026 — Waldemar Link Waldemar Link Hello, I own a Waldemar Link that is covered by recall Z-1511-2026 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.
