# FDA recall Z-2540-2018

> **OMNIlife science Inc.** · Class II · device recall initiated 2018-05-18.

## Product

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

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-2540-2018
- **Recalling firm:** OMNIlife science Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-18
- **Report date:** 2018-08-01
- **Termination date:** 2019-01-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Raynham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2540-2018

## Citation

> AI Analytics. FDA recall Z-2540-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2540-2018. Source: US FDA. Licensed CC0.

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