DJO Surgical recalls hip implants (Size#3) with potential infection risk. Affected units have specific UDI-DI/Lot/Expiration codes. Contact for details on safety.
Orthopedic device components were not subjected to final sterilization before shipment, which if implanted may lead to varying degrees of infection, which may require treatment, prolonged monitoring, and may lead to revision surgery
DJO Surgical is recalling hip implants that may not have been properly sterilized before shipping. If implanted, these parts could cause infections requiring treatment, monitoring, and possible surgery.
The hip implants were not fully sterilized before shipment. If implanted, they could lead to infections that might need antibiotics, extra monitoring, and possibly surgery to fix the problem.
Patients who received the recalled hip implants (Size#3) with the specific UDI-DI/Lot/Expiration codes listed. Those with the implant are at risk of infection.
Check for the UDI-DI/Lot/Expiration codes: 00888912079631/415N1014/May 3, 2028 on the implant packaging or device. The product is a hip implant (Size#3) from DJO Surgical.
Look for the UDI-DI/Lot/Expiration code 00888912079631/415N1014/May 3, 2028 on the implant packaging or device.
The hip implants were not fully sterilized before shipment, which could lead to infections if implanted.
Check the UDI-DI/Lot/Expiration code on the implant. If it matches 00888912079631/415N1014/May 3, 2028, contact DJO Surgical for further instructions.
The implant may cause infections requiring treatment, monitoring, and possible surgery if not properly sterilized.
We’ve drafted a message you can send DJO Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2605-2023 — DJO Surgical DJO Surgical Hello, I own a DJO Surgical that is covered by recall Z-2605-2023 from DJO Surgical. 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.
