Zimmer Biomet recalls certain intramedullary fixation guide wires due to potential creases compromising sterility. Affected items expire before Sept 30, 2023. No remedy specified in official notice.
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 surgical guide wires that may have creases in the sealing area, which could compromise sterility. This is a safety concern for medical procedures where sterile instruments are critical.
Creases in the sealing area opposite the chevron opening could allow contamination, compromising the instrument's sterility. This risk is critical during surgical procedures where infection could occur.
Orthopaedic surgeons and medical facilities using the recalled guide wires for surgery. Patients undergoing procedures with these instruments may be at risk if the wires are not sterile.
The product is a Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire with bullet tip, 3.0 mm diameter, 100 cm length. Item number 47-2237-038-00. All lots expiring before September 30, 2023.
Identify if your guide wire matches the description: bullet tip, 3.0 mm diameter, 100 cm length, item number 47-2237-038-00, and expires before September 30, 2023.
The official recall notice states that creases may compromise sterility, so it is not safe to use without verification.
The recall notice does not specify a remedy, so contact Zimmer Biomet directly for guidance.
Look for the item number 47-2237-038-00 and expiration date before 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-0535-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0535-2019 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.
