BioPro recalls ceramic femoral head implants (28-30mm) due to potential packaging defects that could compromise sterility, risking infection after implantation.
Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
BioPro is recalling ceramic femoral head implants (28-30mm) because packaging issues might compromise sterility, increasing infection risk if implanted. This recall affects patients who have received these specific implants during surgery.
The packaging may have defects that compromise the sterile barrier, which could lead to loss of sterility. If the implant is placed inside the body, this might cause infection after surgery.
Patients who received the recalled ceramic femoral head implants (28-30mm) during surgery are affected. Surgeons and medical facilities using these implants are at risk of potential infection if the device is implanted.
Check if your implant has a product ID of 19023, 19024, 19025, 19026, or 19027 with a specific size (28mm or 32mm). All lots and serial numbers are affected.
Reach out to your surgeon to confirm if you received a recalled implant and discuss next steps.
No, this recall is for surgical implants that may have packaging defects. If you received this implant during surgery, contact your surgeon for guidance.
Check the product ID on your implant: 19023, 19024, 19025, 19026, or 19027 with sizes 28mm or 32mm. All lots and serial numbers are affected.
The recall does not include a fix; affected patients should contact their surgeon for further instructions.
We’ve drafted a message you can send BioPro to request your refund or repair — edit it as you like.
Subject: Recall Z-0151-2026 — BioPro BioPro Hello, I own a BioPro that is covered by recall Z-0151-2026 from BioPro. 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.
