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Aesculap Implant Systems LLC recalls JS Series SterilContainer S2 System
Recalled February 21, 2018 · FDA recall Z-0624-2018 · Aesculap Implant Systems
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. · FDA Class II
Units
292 units
Sold at
Nationally
Description
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.
Product
JS Series SterilContainer S2 System
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →