In2bones USA, LLC recalls
Every recall we track for In2bones USA, LLC — 6 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from In2bones USA, LLC peaked in 2018 (3); 6 since 2017.
All FDA recall records for In2bones USA, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 2 | 0 | 3 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 1 | 0 | 2 |
What to do if you have a recalled In2bones USA, LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All In2bones USA, LLC recalls
5 shown- Use cautionMedical device
In2bones USA, LLC recalls REF: P65 ST862 CoLag SCREW, FT, 6.7X62.5 mm
In2bones USA recalls 29 partially threaded bone screws (model P65 ST862) sold nationwide. Due to labeling error, screws are not fully threaded and may cause injury during surgery.
In2bonesSep 9, 2026 - Lower riskMedical device
In2bones USA, LLC recalls NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic
In2bones USA recalls NeoSpan SuperElastic Compression Staples due to missing Magnetic Resonance Conditional symbol on packaging and labels. This could lead to unsafe MRI scans if used without proper labeling.
In2bonesMay 11, 2026 - Use cautionMedical device
In2bones USA, LLC recalls CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended
In2bones recalls CoLink Bone Graft Harvesters that may break at the outer tube weld site, causing potential injury during surgery. Affected models include REF G05 S1008 with specific lot numbers.
In2bonesAug 18, 2021 - Use cautionMedical device
In2bones USA, LLC recalls NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x10x10, Part Number T50 SN010
In2bones recalls NeoSpan SuperElastic Compression Staple kits with wrong 3mm drill bit (should be 2mm). Affected lots: 9G88C0. Stop using immediately to avoid injury.
In2bonesNov 14, 2018 - Lower riskMedical device
In2bones USA, LLC recalls CoLink(TM) Lapidus Plate XP, +2 mm, Right, REF P40 ST165, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿
In2bones recalls one unit of CoLink Lapidus Plate XP +2mm Right (REF P40 ST1:165) due to incorrect laser marking. This could lead to improper use in orthopedic procedures.
In2bonesJul 16, 2018
In2bones USA, LLC recall questions
How many recalls has In2bones USA, LLC had?
6 recalls from In2bones USA, LLC are on record with U.S. safety agencies, from 2018–2026.
What is the most recent In2bones USA, LLC recall?
In2bones USA, LLC recalls REF: P65 ST862 CoLag SCREW, FT, 6.7X62.5 mm, dated Sep 9, 2026. Every In2bones USA, LLC recall is listed on this page, newest first.
What should I do if I have a recalled In2bones USA, LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new In2bones USA, LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.