Zimmer Biomet recalls certain humeral guide wires due to potential sterility compromise from creases in the sealing area. Affected items have specific model and expiration dates. Consumers should contact the manufacturer 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 specific humeral guide wires used in orthopedic surgery because creases in the sealing area could compromise sterility. This risk could lead to infections if the wires are used without proper sterilization.
Creases in the sealing area on the end of the guide wire opposite the chevron opening can compromise the product's sterility. This means the wires might not be properly sterilized before use, increasing the risk of infection during surgery.
Surgical teams and hospitals that use Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wires with item number 00-2255-026-00. Patients undergoing orthopedic surgery with these instruments are at risk of infection if the wires are not properly sterilized.
Check for the item number 00-2255-026-00 on the packaging. These wires were sold with expiration dates prior to September 30, 2023.
Look for the item number 00-2255-026-00 on the packaging or label.
The recall is due to creases in the sealing area that could compromise sterility, potentially leading to infections during surgery.
Contact Zimmer Biomet directly for details on how to handle the affected product, as the recall remedy is not specified in the record.
Yes, the affected items expire prior to September 30, 2023.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0532-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0532-2019 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.
