Biomet, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1284-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462

Product Classification:

Class II

Date Initiated: February 6, 2023

Date Posted: March 29, 2023

Recall Number: Z-1284-2023

Event ID: 91866

Reason for Recall:

The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.

Status: Ongoing

Product Quantity: 12 units

Code Information:

UDI: (01)00880304703506(17)321128(10)65731960; Lot Number: 65731960

Distribution Pattern:

US Distribution to states of: AZ, FL, GA, MI, NE, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated