Zimmer Biomet recalls certain humeral guide wires due to potential sterility compromise from creases in the sealing area. Affected items were sold before September 30, 2023. No action is required as this is a surgical instrument used in procedures.
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 recall does not affect end-users but is for surgical teams using the product.
Creases in the sealing area opposite the chevron opening may compromise the product's sterility. This could theoretically lead to infection if the wire is used without proper sterility.
Surgical teams using the specific Zimmer M/DN¿ humeral guide wires during orthopedic procedures. Patients receiving the surgery are not directly affected by this recall.
Check for the product name 'Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Smooth, 2.4 mm Diameter, 70 cm Length' with item number 00-2255-025-00. The product was sold before September 30, 2023.
Verify the product name and item number to confirm if it matches the recalled items.
No, this recall is for surgical teams using the product during procedures. Patients are not directly affected.
No action is required as this is a surgical instrument used in procedures. The recall does not affect end-users.
Check the product details to confirm if it matches the recalled items. No action is needed if it does not match.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0531-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0531-2019 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.
