Epic Extremity recalls specific midfoot/flatfoot inserts due to artwork error misidentifying a plate and screw. Affected units include model 2111-0005 lot 51464.
There is an error in the caddy artwork that misidentifies a specific plate and screw.
Epic Extremity is recalling a specific midfoot/flatfoot insert model because artwork incorrectly identifies a plate and screw. This error does not pose a safety risk but requires correction to ensure proper use.
The artwork error misidentifies a specific plate and screw, which could lead to incorrect installation if the user follows the wrong instructions. This does not cause injury but may result in improper function of the orthopedic device.
People who purchased the Epic Extremity Plate System Midfoot/Flatfoot Insert (model 2111-0005, lot 51464) for orthopedic use are affected. Those using the product for foot support are most at risk of incorrect installation.
Check for the model number 2111-0005 and lot number 51464 on the product packaging. The product was sold between 2000 and 5002.
Verify the model number 2111-0005 and lot number 51464 on the packaging to confirm if the product is affected.
No, the recall is for an artwork error that misidentifies a plate and screw, which does not pose a safety risk but requires correction for proper use.
Check the model number and lot number on the packaging to see if it matches 2111-0005 lot 51464. If it does, contact Epic Extremity for guidance.
Look for the model number 2111-0005 and lot number 51464 on the packaging. The product was sold between 2000 and 5002.
We’ve drafted a message you can send Epic Extremity to request your refund or repair — edit it as you like.
Subject: Recall Z-1874-2018 — Epic Extremity Epic Extremity Hello, I own a Epic Extremity that is covered by recall Z-1874-2018 from Epic Extremity. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
