Moximed recalls left and right small knee implants (REF 2-1001/2-1002) due to potential component fracture causing discomfort, swelling, or pain. Affected units sold with specific expiration dates.
Knee implant may fracture due to a supplier-related issue with one component that has nonconforming geometry at the distal end of the absorber component that may result in a reduced wall thickness and microcracks, which may lead to new or worsening symptoms of discomfort, swelling / edema, pain or stiffness, which may necessitate removal of the device.
Moximed is recalling left and right small knee implants (model REF 2-1001 and 2-1002) because a supplier issue may cause the implant to fracture, leading to pain, swelling, or needing removal. This risk affects people who have received these implants with specific expiration dates.
The implant may fracture because of a supplier-related issue with one component that has nonconforming geometry. This can cause reduced wall thickness and microcracks, which might lead to discomfort, swelling, pain, or stiffness that could require the implant to be removed.
People who received the Moximed knee implants with REF numbers 2-1001 or 2-1002 are affected. Those with the specific expiration dates listed in the recall notice are most at risk.
Check for the implant model REF 2-1001 (left) or 2-1002 (right). Look for the expiration dates listed in the recall notice: 29-Mar-25, 21-Sep-25, 26-Mar-26 for REF 2-1001, and 29-Mar-25, 25-Sep-25, 8-Apr-26 for REF 2-1002.
Review the implant's reference number (REF) and expiration date to confirm if it matches the recalled models.
The recall is due to a supplier-related issue with one component that may cause the implant to fracture, leading to discomfort, swelling, pain, or stiffness that could require removal.
The recall notice does not specify a remedy or action for affected users. Check the implant's reference number and expiration date to confirm if it is recalled.
Your implant is affected if it has REF 2-1001 (left) or 2-1002 (right) with the specific expiration dates listed in the recall notice.
We’ve drafted a message you can send Moximed to request your refund or repair — edit it as you like.
Subject: Recall Z-0762-2025 — Moximed Moximed Hello, I own a Moximed that is covered by recall Z-0762-2025 from Moximed. 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.
