Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER Recalled by Aesculap Implant Systems LLC Due to Set screwdriver fails during surgery by deforming at...
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 Aesculap Implant Systems LLC directly.
Affected Products
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
Quantity: 9 pieces
Why Was This Recalled?
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
Where Was This Sold?
This product was distributed to 6 states: CA, FL, GA, IL, MI, OH
About Aesculap Implant Systems LLC
Aesculap Implant Systems LLC has 61 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report