Nextremity Solutions recalls orthopedic surgical instruments Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU NX-4532K-SC due to oversized driver causing surgery delays. Affected units have specific lot numbers and UDI.
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 two orthopedic surgical instruments that may cause delays in surgery because the driver's proximal end is oversized. This could lead to longer procedures and increased risks for patients.
The proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant. This can cause delays in surgery, potentially increasing risks for patients during procedures.
Orthopedic surgeons and hospitals using the Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU NX-4532K-SC are likely affected. Patients undergoing surgery with these instruments face potential delays.
Check for the SKU NX-4532K-SC on the instrument. Affected units have lot numbers 168117318C or 168125017D and UDI 00817701020004.
Verify the SKU, lot number, and UDI to confirm if your instrument is affected.
The 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.
The recall record does not specify a remedy, so check the instrument details to confirm if it's affected.
Look for SKU NX-4532K-SC, lot numbers 168117318C or 168125017D, and UDI 00817701020004.
We’ve drafted a message you can send Nextremity Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-0911-2022 — Nextremity Solutions Nextremity Solutions Hello, I own a Nextremity Solutions that is covered by recall Z-0911-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
