Nextremity Solutions recalls its Nextra CH Cannulated Hammertoe Mini Instrument Kit for potential surgical complications. The device may deform the implant locking mechanism during insertion, leading to delays or revision surgery.
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 its Nextra CH Cannulated Hammertoe Mini Instrument Kit because it can cause improper implant fitting during surgery. This may lead to surgical delays, removal of the implant, or needing a different surgical approach.
The device may deform the implant locking mechanism when inserted into bone. This can cause the implants to not fit properly, leading to surgical delays, removal of the implant, or needing a different surgical approach.
Surgical patients who received the Nextra CH Cannulated Hammertoe Mini Instrument Kit for toe repair are affected. Patients who had the kit used in their surgery are most at risk.
Check for the SKU: CH-MINI-KT and Lot Number: 1578401 on the kit. The UDI is 00817701026389. This kit is used for small bone reconstruction in the toes.
Reach out to Nextremity Solutions directly for guidance on the recall.
The recall states the kit may cause improper implant fitting during surgery, leading to delays or revision procedures.
The recall does not specify a remedy, so contact Nextremity Solutions directly for guidance.
Look for SKU: CH-MINI-KT, Lot Number: 1578401, and UDI: 00817701026389 on the kit.
We’ve drafted a message you can send Nextremity Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-0739-2022 — Nextremity Solutions Nextremity Solutions Hello, I own a Nextremity Solutions that is covered by recall Z-0739-2022 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.
