Zimmer Biomet recalls specific tear drop guide wires due to potential sterility compromise from creases in sealing areas. Affected items expire before Sept 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 certain tear drop guide wires used in orthopedic surgery because creases in the sealing area could compromise sterility. This means the surgical instruments might not be sterile when used, risking infection during procedures.
Creases in the sealing area opposite the chevron opening can compromise the product's sterility. This means the surgical instrument might not be sterile when used during procedures, potentially leading to infection.
Orthopedic surgeons and surgical teams using the specific tear drop guide wires with item number 47-2490-098-01. The risk is highest for procedures where sterility is critical.
Check for the item number 47-2490-098-01 on the packaging. The product is a single-use surgical instrument for orthopedic procedures and expires before September 30, 2023.
Look for the item number 47-2490-098-01 on the packaging or label.
The recall indicates potential sterility issues, so it's not recommended for use until the remedy is applied. Zimmer Biomet has not provided a specific remedy for this product.
Check for the item number 47-2490-098-01 on the packaging. The product expires before September 30, 2023.
Zimmer Biomet has not provided a specific remedy for this product, so contact them 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-0541-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0541-2019 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.
