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Aesculap Implant Systems LLC recalls RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Recalled July 27, 2022 · FDA recall Z-1405-2022 · Aesculap Implant Systems
Hazard
Customized coronal rod benders may deform the implant when used with the spinal system devices. · FDA Class II
Units
2 pieces
Sold at
United States: CO
Description
Customized coronal rod benders may deform the implant when used with the spinal system devices.
Product
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →