FDA-Device2018-02-21Class II
JS Series SterilContainer S2 System
Aesculap Implant Systems LLC
Hazard
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.
Sold states
Nationally
Affected count
292 units
Manufactured in
3773 Corporate Pkwy, Center Valley, PA, United States
Products
JS Series SterilContainer S2 System
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0624-2018Don't want to check this manually?
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