Zimmer recalls certain hip implants that contain a smaller size than labeled, which could lead to improper fit and complications. Affected packages have specific part and lot numbers.
Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip implant, actually contained a Size 4 Standard Reduced Neck length taper hip implant.
Zimmer is recalling hip implants that were shipped with the wrong size (Size 4 instead of Size 7.5). This mismatch could cause improper fit and potential complications during surgery. The recall affects specific packages with known part and lot numbers.
The recalled implants were labeled as Size 7.5 but contained a smaller Size 4 implant. This size mismatch could lead to improper fit during surgery, potentially causing complications like improper alignment or instability.
Patients who received the recalled hip implants from specific lot numbers and part numbers are affected. Surgeons and hospitals that used these implants are at risk of complications.
Check the package for part number 00-7711-004-10 and lot numbers 63716613 or 63716614. The unique device identifier (UDI) starts with (01)00889024131606.
Look for part number 00-7711-004-10 and lot numbers 63716613 or 63716614 on the implant package.
The recall is happening because some packages labeled as Size 7.5 actually contained a Size 4 implant, which could lead to improper fit during surgery.
Check for part number 00-7711-004-10 and lot numbers 63716613 or 63716614 on the implant package.
The recall record does not specify a remedy, so contact Zimmer Biomet directly for guidance.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-1192-2018 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-1192-2018 from Zimmer. 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.
