K2M recalls Yukon Polyaxial Screw Size 4.0x26mm (catalog 7601-04026) due to incorrect laser marking. This may lead to improper spinal surgery use. Affected units have lot number KRBX.
The Yukon polyaxial screw used in the Yukon Spinal System was incorrectly laser marked with size 5.0 mm (diameter) & 24 mm (length).
K2M recalls a specific spinal screw component that was incorrectly marked with size 5.0 mm and 24 mm measurements instead of the correct 4.0x26mm. This could cause improper surgical use if the wrong size is selected during spinal procedures.
The screw was laser marked with the wrong size (5.0 mm diameter and 24 mm length) instead of the correct 4.0x26mm specifications. This mismatch could lead to improper surgical implantation if the wrong screw size is used during spinal procedures.
Patients undergoing spinal surgery who use the Yukon Spinal System with this specific screw component are affected. Surgeons and medical staff who handle the recalled screws are at risk of using incorrect measurements during procedures.
Check for the catalog number 7601-04026 on the screw packaging or label. Affected units have lot number KRBX. This screw is part of the YUKON Spinal System.
Look for the catalog number 7601-04026 and lot number KRBX on the screw packaging or label.
The recall indicates the screw was incorrectly marked, which could lead to improper surgical use if the wrong size is selected. However, the hazard is not described as causing immediate injury or death in normal use.
The recall does not specify a remedy, so you should contact K2M directly to confirm if your specific unit is affected and what actions to take.
Check for the catalog number 7601-04026 and lot number KRBX on the screw packaging or label. This screw is part of the YUKON Spinal System.
We’ve drafted a message you can send K2M to request your refund or repair — edit it as you like.
Subject: Recall Z-0931-2021 — K2M K2M Hello, I own a K2M that is covered by recall Z-0931-2021 from K2M. 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.
