Overview of recall records associated with In2bones USA, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 5.
Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.
Complaints were received of CoLink Bone Graft Harvesters breaking at the outer tube weld site.
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.
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…
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…
This page summarizes recall records in which the official source identifies In2bones USA, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
