Nextrem: Nextra Hammertoe Correction System Driver (SKU NX-DR) has an oversized proximal end causing surgery delays. Affected units: Lot 168A27917C. Contact manufacturer for remedy.
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Nextremity Solutions is recalling their Nextra Hammertoe Correction System Driver (SKU NX-DR) because the driver's proximal end is oversized, which can cause delays during surgery. This is a serious issue for orthopedic procedures where timing is critical.
The driver's proximal end is oversized in varying degrees, making it difficult to fully connect and remove from the Nextra implant. This can cause delays in surgery, which is critical for orthopedic procedures where timing affects patient outcomes.
Orthopedic surgeons and medical facilities using the Nextra Hammertoe Correction System Driver (SKU NX-DR) with Lot Number 168A27917C are affected. Surgeons using this specific model during procedures are at risk of delayed surgery.
Check for the SKU NX-DR on the driver. Affected units have Lot Number 168A27917C. This product was sold as an orthopedic surgical instrument.
Look for Lot Number 168A27917C on the driver's packaging or label.
The driver may cause surgery delays due to an oversized proximal end, but it does not pose an immediate risk of injury or death.
Check for SKU NX-DR and Lot Number 168A27917C on the driver's packaging or label.
The recall record does not specify a remedy, so contact Nextremity Solutions directly for guidance.
We’ve drafted a message you can send Nextremity Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-0914-2022 — Nextremity Solutions Nextremity Solutions Hello, I own a Nextremity Solutions that is covered by recall Z-0914-2022 from Nextremity Solutions. 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.
