Aesculap Implant Systems LLC recalls RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal
Recalled Product
RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Hazard / Issue
Customized coronal rod benders may deform the implant when used with the spinal system devices.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: LOT: 2930902A
View official government recall
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