Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of Recalled by Aesculap Implant Systems LLC Due to The NS357R Vega PS Tibia Trial/Preparation Plateau size...
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
NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of the Vega Knee System Set #ST0468) The affected part is provided in the Vega Knee System Set #ST0468. The Vega Knee System is used for reconstruction of the diseased knee joint.
Quantity: 13 Units
Why Was This Recalled?
The NS357R Vega PS Tibia Trial/Preparation Plateau size T4 may be incorrectly labeled. If the incorrect size trial is used the potential risk is implantation of the incorrect implant size which may lead to injury of ligaments, pain and possible revision surgery.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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