Zimmer Biomet recalls hip replacement cups made with untested sterilant that may cause tissue reactions. Affected units include specific model and all lots. Consumers should contact for details.
Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis component was not evaluated to confirm the biocompatibility of the residual sterilant. Cannot rule out the potential for adverse tissue reactions.
Zimmer Biomet is recalling hip replacement cups that may contain untested sterilant, potentially causing tissue reactions. This affects patients who received the specific cup model. Immediate contact with the company is needed for details.
The hip cup was sterilized using hydrogen peroxide, but the residual sterilant wasn't tested for biocompatibility. This could lead to adverse tissue reactions if the sterilant causes an immune response.
Patients who received the recalled hip cup model are most at risk. The recall applies to all units of this specific cup design.
Check for the model name 'ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D. Cup with Spacers, 51 mm'. All lots of this specific model are affected.
Reach out to Zimmer Biomet directly for specific instructions on handling the recalled hip cup.
The recall states there's a potential for adverse tissue reactions, but it cannot rule out the possibility. The exact risk level isn't specified.
Check for the model name 'ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D. Cup with Spacers, 51 mm'. All lots of this model are affected.
Contact Zimmer Biomet directly for specific instructions on handling the recalled hip cup.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0370-2021 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0370-2021 from Zimmer Biomet. 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.
