In2Bones Non-Locking Screws Recall: Risk of Fracture During Surgery
In2Bones recalls specific lengths of Non-Locking screws used in distal radius fracture repairs due to reported perioperative breakages during surgery.
Lower-risk recall
The firm received several customer complaints reporting some perioperative breakages of NE0411 Non-Locking screws when inserting the screw into the radius diaphysis
Contact the company
What happened, in plain English
In2Bones is recalling certain lengths of Non-Locking screws used in distal radius fracture repairs because they have broken during surgery. This could lead to complications if the screws fail while being inserted into the bone. Read more at govinfonow.com/recall/73429-in2bones-non-locking-screws-recall-risk-of-fracture-during-surgery.
Source Summary by GovInfoNow · govinfonow.com/recall/73429-in2bones-non-locking-screws-recall-risk-of-fracture-during-surgery · Updated September 20, 2026 · FDA enforcement record: FDA #Z-2869-2017
Cite this page
“In2Bones Non-Locking Screws Recall: Risk of Fracture During Surgery.” GovInfoNow, updated September 20, 2026. https://govinfonow.com/recall/73429-in2bones-non-locking-screws-recall-risk-of-fracture-during-surgery. Based on FDA recall #Z-2869-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2869-2017%22&limit=1).
Why it’s dangerous
The screws have been reported to break during insertion into the radius bone, which could cause complications during surgery. This issue occurs when the screws are used in the specific lengths and models listed in the recall.
Who’s affected
Orthopedic surgeons and medical professionals who use In2Bones NEOVIEW Plating Systems for distal radius fractures. Patients receiving this specific surgical procedure are at risk if the recalled screws are used.
How to tell if you have this one
Check if your screws are labeled NEO(R) 0.27 - 10 mm (REF W27 ST010), NEO(R) 0.27 - 12 mm (REF W27 ST012), or other lengths listed in the recall notice. These screws are part of the NEOVIEW Plating System for distal radius fractures.
- Brand
In2Bones- Category
Medical device
What to do — step by step
Check Screw Details
Identify if your screws match the recalled lengths and reference numbers listed in the recall notice.
Where it went and when
Where it was distributed
Distributed in Tennessee, and outside the U.S.
FDA distribution: “Worldwide Diribution - US including Tennessee; Foreign - Italy, Portugal, Spain, Switzerland, UK, and France” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Tennessee.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-2869-2017 (July 13, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2869-2017 to see it in context.
- Plain-language summary written by qwen3:4b on September 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.