Exactech, Inc.: Medical Device Recall in 2021 - (Recall #: Z-2126-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 136-28-XX, Novation GXL Liner, +5mm Lateralized, 28mm; and Novation GXL Liner, +5mm Lateralized, G0, 22mm ID. Orthopedic hip implant component.

Product Classification:

Class II

Date Initiated: June 29, 2021

Date Posted: July 28, 2021

Recall Number: Z-2126-2021

Event ID: 88126

Reason for Recall:

Risk of edge-loading and premature prosthesis wear is possible in a specific subset of patients with certain implant configurations and surgical implant positioning.

Status: Ongoing

Product Quantity: 89,050 total

Code Information:

All serial numbers. UDI-DI numbers: 10885862024213, 10885862024220, 10885862024237

Distribution Pattern:

Distribution US nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated