K2M, Inc recalls Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-
Recalled Product
Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068
Hazard / Issue
Units may arrive with missing pins and/or in a state in disassembly. Pins dislodging from the instrument during a procedure may enter the surgical cavity, requiring intraoperative removal or revision surgery.
Issued by
FDA
Affected States: CO, IL, LA, MA, MS, OK, PA, TN, TX
Lot/Code Info: Lots CCUNA, HYMJ, KNCU
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