K2M recalls Yukon Anti-Torque Alignment Tube (Lot KTGG) due to potential surgery delays. Affected users should contact K2M for details.
Shafts do not pass through the inner cannula of the Anti-Torque Alignment Tube from Lot KTGG due to a manufacturing nonconformance. This could result in a delay of surgery or result in surgical intervention later on.
K2M is recalling a specific spinal surgery tool that may cause surgery delays if used improperly. This affects medical professionals who use the product during spinal procedures.
The alignment tube's shaft does not pass through the inner cannula properly in Lot KTGG units. This could cause delays in surgery or require additional surgical steps later.
Medical professionals using the Yukon Anti-Torque Alignment Tube for spinal surgery. The risk is highest for those using the product during procedures involving Lot KTGG.
Check if your product has the catalog number 7601-90001 and lot number KTGG. The product was sold with GTIN 10888857343948.
Reach out to K2M directly for specific instructions about the recalled product.
The recall indicates a potential risk of surgery delays or additional procedures, but it does not describe immediate injury risks.
Look for catalog number 7601-90001 and lot number KTGG on the product label.
Contact K2M directly for specific instructions about the recalled product.
We’ve drafted a message you can send K2M to request your refund or repair — edit it as you like.
Subject: Recall Z-0520-2021 — K2M K2M Hello, I own a K2M that is covered by recall Z-0520-2021 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.
