Zimmer Biomet recalls certain intramedullary guide wires due to potential sterility compromise from creases in the sealing area. Affected items have specific model and expiration dates.
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 used in orthopedic surgery because creases in the sealing area could compromise sterility. This risk affects surgical instruments that expired before September 30, 2023.
Creases in the sealing area opposite the chevron opening could compromise the product's sterility. This means the instrument might not be sterile when used in surgery, potentially leading to infections.
Orthopedic surgeons and hospitals using the recalled guide wires for surgical procedures. The risk is low as this is a single-use instrument with no direct injury mechanism.
Check for the product name 'Zimmer ZMS Intramedullary Fixation Smooth Guide Wire', 3.0 mm diameter, 100 cm length, with item number 47-2237-037-00. The instrument expired before September 30, 2023.
Verify the expiration date is before September 30, 2023.
The recall indicates potential sterility issues, but the product is safe for use if it has not been compromised by creases in the sealing area.
Look for the specific model: Zimmer ZMS Intramedullary Fixation Smooth Guide Wire, 3.0 mm diameter, 100 cm length, item number 47-2237-037-00, with an expiration date before September 30, 2023.
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-0534-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0534-2019 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.
