Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Chesapeake Anterior Lumbar (AL) Removal Tool Recalled by K2M, Inc Due to Units may arrive with missing pins and/or in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact K2M, Inc directly.
Affected Products
Chesapeake Anterior Lumbar (AL) Removal Tool; Cat. no. 2008-90068
Quantity: 23
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 9 states: CO, IL, LA, MA, MS, OK, PA, TN, TX
About K2M, Inc
K2M, Inc has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report