OMNIlife recalls hip replacement model HC-00070 due to missing porous coating. This could affect bone integration. Affected users should contact for remedy.
Stems missing porous coating on the device.
OMNIl:ife recalls hip replacement implants with model HC-00070 because they lack a critical porous coating. This may cause poor bone healing and long-term failure of the implant.
The hip implant lacks a porous coating that helps bones grow into it. Without this coating, the implant may not bond properly with bone, leading to loosening or failure over time.
Patients who received the OMNI Hip System model HC-00070 for hip replacement surgery are affected. Those with the implant are most at risk.
Check for the model HC-00070, catalogue number, or order number HC-00070 on the implant. The lot number 33035 is also associated with this recall.
Reach out to OMNIlife science Inc. for guidance on next steps.
The recall is for missing porous coating, which may affect bone integration but does not cause immediate harm. The risk is long-term.
Check the implant for model HC-00070, catalogue number, or order number HC-00070. Lot number 33035 is also associated with this recall.
Contact OMNIlife science Inc. for guidance on next steps.
We’ve drafted a message you can send OMNIlife to request your refund or repair — edit it as you like.
Subject: Recall Z-0169-2020 — OMNIlife OMNIlife Hello, I own a OMNIlife that is covered by recall Z-0169-2020 from OMNIlife. 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.
