Zimmer Biomet recalls Humeral Stem 83mm (Size 17) due to incorrect lot numbers causing size mismatch. Affected patients should contact the manufacturer for guidance.
Zimmer Biomet is conducting a medical device recall for two lots of Comprehensive Humeral stems. The lots were commingled during the manufacturing process and were etched with incorrect lot numbers. The size difference between the two stem sizes is 1.1 inches. It is visually recognizable by the user that the box label does not match the contents of the box.
Zimmer Biomet is recalling Humeral Stem 83mm (Size 17) implants because manufacturing errors led to incorrect lot numbers. This size difference (1.1 inches) can cause improper fit during surgery, potentially leading to complications.
The recall involves two lots of stems that were mixed during manufacturing and labeled with wrong lot numbers. The size difference between the stems is 1.1 inches, which could lead to improper surgical fit if used in procedures requiring precise sizing.
Patients who received the Humeral Stem 83mm (Size 17) implant during surgery are affected. Surgeons and medical staff who used these implants are at higher risk.
Check the box label for the product name and size. The affected stems have a size difference of 1.1 inches and the box label does not match the contents.
Reach out to Zimmer Biomet directly for guidance on next steps after identifying the recalled implant.
The recall occurs because two lots of stems were mixed during manufacturing and labeled with incorrect lot numbers, causing a 1.1-inch size difference.
The box label does not match the contents of the box, and the stems have a 1.1-inch size difference.
Contact Zimmer Biomet directly for guidance on next steps after identifying the recalled implant.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0979-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0979-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
