fda
2 records
FDA Device Recall: NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x10x10, Part Numbe
2019-01-02
Class II — 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.
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FDA Device Recall: CoLink(TM) Lapidus Plate XP, +2 mm, Right, REF P40 ST165, QTY 1, In2Bones Pr
2018-08-29
Class II — 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 pla...
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