Zimmer Biomet recalls tear drop guide wires with potential sterility issues. Affected items have creases in the sealing area that could compromise product sterility. Consumers should contact the company for details.
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 a specific surgical guide wire due to potential creases in the sealing area that could compromise sterility. This risk affects the safety of the product during orthopaedic surgery.
The guide wire has creases in the sealing area opposite the chevron opening, which could compromise the product's sterility. This means the surgical instrument might not be sterile when used, potentially leading to infections during procedures.
Orthopaedic surgeons and medical professionals using the Zimmer Natural Nail Tear Drop Guide Wire for surgical procedures. The risk is primarily for those using the specific product in clinical settings.
Check for the product name 'Zimmer Natural Nail Tear Drop Guide Wire', 2.4 mm diameter, 100 cm length, and item number 47-2490-097-01. The product expires before September 30, 2023.
Reach out to Zimmer Biomet directly for specific instructions on handling the recalled item.
The recall indicates potential sterility issues, so it is not recommended for use until the manufacturer provides further guidance.
Check for the product name 'Zimmer Natural Nail Tear Drop Guide Wire', 2.4 mm diameter, 100 cm length, and item number 47-2490-097-01.
Contact Zimmer Biomet directly for specific instructions on handling the recalled item.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0539-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0539-2019 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.
