medical MODERATE Updated 2018-02-07

Exactech, Inc. recalls Equinoxe Cage, Glenoid, Alpha, Small Product Usage: The

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Recalled Product

Equinoxe Cage, Glenoid, Alpha, Small 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.

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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: 5013050 - 5013079

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
View official government recall