Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The MectaLIF Oblique Handle Recalled by Medacta Usa Due to The MectaLIF Oblique Handle has the laser marking...
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 Medacta Usa directly.
Affected Products
The MectaLIF Oblique Handle, model number 03.22.10.0262, is used to insert the MectaLIF oblique spinal cage implants.
Quantity: 32 oblique handles
Why Was This Recalled?
The MectaLIF Oblique Handle has the laser marking "MEDIAL" on the incorrect side and could result in incorrect insertion of the device during surgery.
Where Was This Sold?
This product was distributed to 3 states: CA, CO, ID
About Medacta Usa
Medacta Usa has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report