Biomet, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1925-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

DISCOVERY ELBOW prosthesis, 4 MM X 100 MM RIGHT HUMERAL FLANGED I BOND COAT Tl 6AL 4V ALLOY. Elbow joint replacement prostheses are intended for primary and revision joint arthroplasty for use in cemented applications.

Product Classification:

Class II

Date Initiated: May 15, 2014

Date Posted: July 2, 2014

Recall Number: Z-1925-2014

Event ID: 68418

Reason for Recall:

Surface finish is different than specified. The implant has 30 grit blast on the exterior of the flange when the print calls for the glass bead blast. The patient may experience pain requiring surgical intervention.

Status: Terminated

Product Quantity: 1

Code Information:

Catalog/REF #: 114905, Lot #: M846640

Distribution Pattern:

US Nationwide Distribution in the state of California

Voluntary or Mandated:

Voluntary: Firm initiated