Home / Recalls / Medical Devices
Aesculap Implant Systems LLC recalls Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the l
Recalled September 7, 2022 · FDA recall Z-1638-2022 · Aesculap Implant Systems
Hazard
Potential for the incorrect screw to be included in the package. · FDA Class II
Units
6 units
Sold at
GA, TX
Description
Potential for the incorrect screw to be included in the package.
Product
Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar, thoracic and sacral spine. Article Number: 52758014
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →