MicroPort Orthopedics recalls specific knee implant components due to potential incorrect packaging. Affected items may have wrong labeling, but no injury reports. Consumers should check model numbers and contact for details.
Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
MicroPort Orthopedics is recalling certain knee implant components because they might have incorrect packaging labels. This could lead to improper use if the wrong part is installed. The recall does not involve injuries or immediate safety risks.
The implants may have incorrect packaging labels, which could lead to using the wrong component during surgery. However, the recall states that the devices themselves have correct markings, so the risk is limited to labeling errors during the implant process.
Patients who received the specific knee implant components with model numbers EFSRP5PR or EFSRN6PL are likely affected. Surgeons and medical facilities using these components are at higher risk for potential mislabeling.
Check for model numbers EFSRP5PR or EFSRN6PL on the packaging. These components were sold with specific expiration dates and lot numbers between 2007 and 2032.
Look for model numbers EFSRP5PR or EFSRN6PL on the packaging to confirm if the item is affected.
The recall record does not mention any injuries or incidents.
The recall does not specify a remedy, so contact MicroPort Orthopedics directly for further instructions.
Check the packaging for model numbers EFSRP5PR or EFSRN6PL, which were sold with specific expiration dates between 2007 and 2032.
We’ve drafted a message you can send MicroPort to request your refund or repair — edit it as you like.
Subject: Recall Z-0699-2025 — MicroPort MicroPort Hello, I own a MicroPort that is covered by recall Z-0699-2025 from MicroPort. 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.
