Biomet, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2483-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.

Product Classification:

Class II

Date Initiated: July 28, 2015

Date Posted: September 9, 2015

Recall Number: Z-2483-2015

Event ID: 71850

Reason for Recall:

The device was assembled without screw hole plugs.

Status: Terminated

Product Quantity: 5

Code Information:

Part Number:135250; Lot Number:946410

Distribution Pattern:

Distributed in Canada and Japan.

Voluntary or Mandated:

Voluntary: Firm initiated