DJO recalls a specific porous knee surgical system due to incorrect product packaging. Affected units have model numbers 243-01-108 and 353-03-108. Consumers should contact DJO for details.
Due to incorrect product/device within packaging.
DJO is recalling a specific porous knee surgical system model because the packaging contains the wrong product. This could lead to incorrect surgical use if the wrong item is installed.
The packaging contains the incorrect product, which could lead to using the wrong surgical component during knee replacement procedures. This might cause improper fitting or function of the implant.
Patients who received this specific knee surgical system model during procedures. Surgeons and medical staff using the product are most at risk of using the wrong item.
Check for model numbers 243-01-108 or 353-03-108 on the packaging. The product was sold with lot numbers 277W1114 or 213W1051.
Look for model numbers 243-01-108 or 353-03-108 on the packaging.
The recall states the packaging contains the incorrect product, so it is not safe to use as intended.
Check for model numbers 243-01-108 or 353-03-108 on the packaging with lot numbers 277W1114 or 213W1051.
The recall does not specify a remedy, so contact DJO directly for guidance.
We’ve drafted a message you can send DJO to request your refund or repair — edit it as you like.
Subject: Recall Z-0508-2024 — DJO DJO Hello, I own a DJO that is covered by recall Z-0508-2024 from DJO. 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.
