In2bones USA Recalls
5 recalls on record · August 29, 2018 to June 17, 2026 · Medical Devices
Recalls by year
18
19
21
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 17, 2026Medical DevicesFDA
In2bones USA, LLC recalls NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElasti
Hazard: Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.
September 29, 2021Medical DevicesFDA
In2bones USA, LLC recalls CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended f
Hazard: Complaints were received of CoLink Bone Graft Harvesters breaking at the outer tube weld site.
January 2, 2019Medical DevicesFDA
In2bones USA, LLC recalls NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x10x10, Part Number T50 SN010
Hazard: The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit. They contain a 3mm drill bit instead of a 2mm drill bit.
August 29, 2018Medical DevicesFDA
In2bones USA, LLC recalls CoLink(TM) Lapidus Plate XP, +2 mm, Left, REF P40 ST265, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLin
Hazard: CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly. In these lots, right plates were laser marked as left plates and the left plates were laser marked as right plates.
August 29, 2018Medical DevicesFDA
In2bones USA, LLC recalls CoLink(TM) Lapidus Plate XP, +2 mm, Right, REF P40 ST165, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLi
Hazard: CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly. In these lots, right plates were laser marked as left plates and the left plates were laser marked as right plates.