Zimmer Biomet recalls certain G-PIN guide wires due to potential sterile barrier breaches causing infection risk. Affected items have specific model numbers and were sold in the US. Consumers should contact the company for details.
The firm is recalling various trauma guide wires due to insufficient packaging design verification and exceeding the expected occurrence rate of complaints for sterile barrier failure. Guide wires packaged in the affected packaging configuration have the potential for sterile barrier breach, leading to possible risk for infection.
Zimmer Biomet is recalling specific G-PIN guide wires that could lead to infection if sterile barriers are breached during use. This recall affects medical devices used in bone surgery procedures.
The guide wires are packaged in a configuration that may not properly seal the sterile barrier. If the barrier is breached during use, it could allow bacteria to enter the surgical site, leading to infection.
Medical professionals who use these guide wires for bone surgery procedures are most at risk. Patients receiving these devices during surgery may also be affected.
Check for model numbers 467265, 554260, 595180, 700960, 828070, 845960, 244870, 002630, 086190, 298890, 754200, 342500, 384400, 662420, 934740, 643860, 547310, 977760, 469890, 399260. These items were sold in the US for bone surgery procedures.
Identify the model number on the packaging or device to confirm if it is affected.
Reach out to Zimmer Biomet for specific instructions on how to handle the recalled items.
Zimmer Biomet is recalling these guide wires due to potential sterile barrier breaches that could lead to infection risk during surgery.
The affected model numbers include 467265, 554260, 595180, 700960, 828070, 845960, 244870, 002630, 086190, 298890, 754200, 342500, 384400, 662420, 934740, 643860, 547310, 977760, 469890, 399260.
Check the model number on the packaging or device. These items were sold in the US for bone surgery procedures.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2236-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2236-2018 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.
