Nextremity Solutions recalls Nextra Cannulated Hammertoe Standard Instrument Kit (SKU: CH-STD-KT) due to risk of surgical delay, implant removal, or revision surgery after improper implant fixation.
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision
Nextremity Solutions is recalling their Nextra Cannulated Hammertoe Standard Instrument Kit for small bone reconstruction. The kit may cause surgical delays, implant removal, or revision surgery if the implant locking mechanism deforms during insertion.
During implant insertion, the driver may deform the implant's locking mechanism. This causes inadequate force between the middle and proximal phalanx implants, leading to surgical complications like delays, removal, or revision procedures.
Surgical patients who received this specific kit for hammertoe repair are affected. Patients who had the kit used during surgery are most at risk.
Check for the product name 'Nextra Cannulated Hammertoe Standard Instrument Kit' (SKU: CH-STD-KT). Lot numbers 1574701 and 158961 are also associated with this recall.
Reach out to Nextremity Solutions directly for guidance on the recall and potential remedies.
No, this recall specifically applies to the Nextra Cannulated Hammertoe Standard Instrument Kit (SKU: CH-STD-KT) used for small bone reconstruction in inter-digital repair.
Contact Nextremity Solutions directly for guidance on the recall and potential remedies.
Look for the product name 'Nextra Cannulated Hammertoe Standard Instrument Kit' (SKU: CH-STD-KT) and lot numbers 1574701 or 158961.
We’ve drafted a message you can send Nextremity Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-0740-2022 — Nextremity Solutions Nextremity Solutions Hello, I own a Nextremity Solutions that is covered by recall Z-0740-2022 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.
