OMNIlife science Inc.: Medical Device Recall in 2018 - (Recall #: Z-2540-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

OMNI Hip System, ApeX-LNK Acetabular Inserts 0 degree, 4+mm offset, Product Codes: H6-14436, H6-13928 & H6-14836 Product Usage: The Apex Hip System is intended for primary or revision total hip replacement. The femoral hip stems and acetabular cups are intended for uncemented fixation and single use implantation. The Apex Acetabular Cup liners, standard and ApeX-LNK Poly, are intended for use with the Apex Modular Acetabular Cup, in combination with the Apex Modular, Apex K2, Apex K2 mid length or Apex K1 Hip in total hip replacement procedures. The acetabular cup inserts are intended to articulate with a metal (cobalt chromium) or ceramic (alumina) femoral head. These prostheses may be used for the following conditions, as appropriate: Non-inflammatory degenerative joint disease, including osteoarthritis and avascular necrosis Rheumatoid arthritis Correction of functional deformity Congenital dislocation Revision procedures where other treatments or devices have failed

Product Classification:

Class II

Date Initiated: May 18, 2018

Date Posted: August 1, 2018

Recall Number: Z-2540-2018

Event ID: 80406

Reason for Recall:

The Internal packaging, the pouch and patient labels are improperly labeled.

Status: Terminated

Product Quantity: 16 units

Code Information:

Lot Numbers - 29147, 29148 & 29778

Distribution Pattern:

US Nationwide Distribution - in the states of AZ, CA, CO, IL, FL & MA

Voluntary or Mandated:

Voluntary: Firm initiated