Zimmer Biomet recalls specific model of intramedullary guide wire due to potential packaging seal failure. Affected units include lot numbers 63662549 through 63826242. Consumers should check their product details and contact the company for guidance.
Potential failure of sterile packaging seal.
Zimmer Biomet is recalling a specific type of intramedullary guide wire that may have a packaging seal that fails. This could lead to contamination of the sterile product, which is a serious risk for surgical procedures.
The sterile packaging seal might fail, allowing contaminants to enter the product. This could lead to infection or other complications during surgical procedures if the guide wire is not properly sterilized.
Medical professionals using this guide wire for surgeries are most at risk. Patients who have received this specific model during surgery may also be affected.
Check the product label for the item number 47-2237-037-00 and lot numbers listed: 63662549, 63668704, 63696974, 63709171, 63721377, 63731176, 63764550, 63771164, 63781920, 63803595, 63812302, 63817719, 63826242.
Look for the item number 47-2237-037-00 and lot numbers listed in the recall notice.
The recall indicates a potential packaging seal failure, which could lead to contamination. Affected units should not be used until the manufacturer provides guidance.
Check the product label for the item number 47-2237-037-00 and lot numbers: 63662549 through 63826242.
Contact Zimmer Biomet directly to confirm if your specific unit is affected and follow their instructions.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1470-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1470-2018 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.
