Zimmer Biomet recalls specific hip implants due to incorrect size packaging. Patients may receive a smaller implant than labeled, risking improper fit and complications.
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 Biomet is recalling certain hip implants because some packages labeled as size 7.5 actually contain size 4 implants. This mismatch could lead to improper fit and potential complications during surgery.
The hazard occurs because the packaging for the implant incorrectly states a larger size (7.5) but contains a smaller size (4). This mismatch could lead to improper fit during surgery, potentially causing complications.
Patients who received the recalled hip implants (size 7.5 labeled but size 4 actually contained) are most at risk. The recall affects individuals who had surgery with these specific implant models.
Check the implant's part number (00-7711-007-40), lot number (63716611), and UDI code (01)00889024131736(17)270731(10)63716611. The implant is part of the Zimmer M/L Taper Hip Prosthesis 7711 Series.
Review the part number, lot number, and UDI code on the implant packaging to confirm if it matches the recalled model.
The recall occurs because some packages labeled as size 7.5 actually contain size 4 implants, which could lead to improper fit during surgery.
Check the implant's part number, lot number, and UDI code to see if it matches the recalled model. Contact Zimmer Biomet for further guidance.
The recall addresses a potential fit issue, but the official notice does not specify a risk of serious injury. This is a low-risk situation.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1191-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1191-2018 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.
