FDASeptember 8, 2021device

Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

k2m

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068 — Recall Details · AllClear