Zimmer Biomet recalls certain intramedullary guide wires due to potential sterility compromise from creases in the sealing area. Affected items have item number 47-2237-033-00 and expire before September 30, 2023.
Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product's chevron opening compromising product sterility
Zimmer Biomet is recalling specific intramedullary guide wires that may have creases in the sealing area, which could compromise sterility during surgery. This risk affects surgical instruments used in orthopedic procedures and requires immediate attention to prevent infection.
Creases in the sealing area opposite the chevron opening can compromise the product's sterility. This means the guide wire may not be sterile when used in surgery, potentially leading to infections in patients.
Orthopedic surgeons and surgical teams using the recalled guide wires for procedures involving prosthesis implantation. Patients undergoing surgery with these instruments are at risk of infection if the sterility is compromised.
Check for the item number 47-2237-033-00 on the packaging. The guide wires expire before September 30, 2023, and are used in orthopedic surgeries for prosthesis implantation.
Look for the item number 47-2237-033-00 and expiration date before September 30, 2023 on the packaging.
Creases in the sealing area opposite the chevron opening can compromise product sterility during surgery.
Check for item number 47-2237-033-00 and expiration date before September 30, 2023 on the packaging.
The recall does not specify a remedy, so contact Zimmer Biomet directly for guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0533-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0533-2019 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.
