Aesculap recalls knee implant components (model nos. NN469K-NN479K) due to potential LDPE particles in packaging. Affected products may have particles that could cause irritation or infection during surgery.
Low Density Polyethylene (LDPE) particles may be present on the surface of the implant upon the opening of the inner packaging.
Aesculap is recalling specific knee implant components (models NN469K to NN479K) because low-density polyethylene particles might be present in the packaging. This could lead to irritation or infection during surgery if the particles are introduced into the surgical site.
Low-density polyethylene (LDPE) particles may be present on the surface of the implant when the inner packaging is opened. These particles could potentially cause irritation or infection if introduced into the surgical site during implantation.
Patients who have received these knee implant components (models NN469K-NN479K) from Aesculap. Surgeons and medical staff using these implants during procedures are at higher risk if particles are present.
Check for model numbers NN469K through NN479K on the packaging. Products with old packaging configuration (before Lot 52533610) are affected. New packaging starts with Lot 52533610.
Look for model numbers NN469K through NN479K and old packaging configuration (before Lot 52533610).
The recall states that LDPE particles may be present, which could cause irritation or infection during surgery. Affected products should be checked and handled with caution.
Check the model numbers and packaging configuration. If affected, contact Aesculap for further instructions.
The hazard is described as potential irritation or infection, not serious injury. The danger level is low risk.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-1480-2020 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-1480-2020 from Aesculap. 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.
