Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
JS Series SterilContainer S2 System Recalled by Aesculap Implant Systems LLC Due to The JS Series SterilContainer S2 System was released...
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
JS Series SterilContainer S2 System
Quantity: 292 units
Why Was This Recalled?
The JS Series SterilContainer S2 System was released to the market place prior to an authorized FDA 510K clearance. No other Aesculap SterilContainer System products are impacted by this recall.
Where Was This Sold?
Nationally
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