Exactech, Inc. recalls Equinoxe Cage, Glenoid, Alpha, Medium Product Usage: The
See all recalls from Exactech, Inc. →Recalled Product
Equinoxe Cage, Glenoid, Alpha, Medium Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint where total or hemi- arthroplasty is determined by the surgeon to be the preferred method of treatment.
Hazard / Issue
Potentially mislabeled.
Issued by
FDA
Affected States: OH, WI, AZ, GA, VA, CA, OK, MN, TN, ME, CO, SC, FL, AL
Lot/Code Info: Catalog #: 314-13-03 Serial Range: 5013020 - 5013049
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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