Zimmer Biomet recalls a specific size 10 hip prosthesis model due to potential safety concerns. Affected customers should contact the company for details on next steps.
See the official notice for the full hazard description.
Zimmer Biomet is recalling a specific size 10 hip prosthesis with Kinective Technology. This recall is due to potential safety concerns that could affect patient safety.
The recall mentions potential safety concerns but does not specify the exact hazard mechanism. Without clear details on what could go wrong, the risk level cannot be determined.
Patients who received this specific hip prosthesis model are likely affected. Those with the size 10 model are at the highest risk.
Check for the model number 00-7713-010-00 or the part numbers 62361460 and 62528141. This specific size 10 hip prosthesis with Kinective Technology is affected.
Reach out to Zimmer Biomet directly for information about the recall and next steps.
The recall mentions potential safety concerns but does not specify the exact hazard mechanism.
Contact Zimmer Biomet directly for information about the recall and next steps.
Check for the model number 00-7713-010-00 or the part numbers 62361460 and 62528141.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2365-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2365-2018 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.
