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Recall Observatory FDA recall evidence

Device 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

Z-2540-2018

May 18, 2018

Class II

Product summary

Firm
OMNIlife science Inc.
Event
Event 80406
Status
Terminated
Classification
Class II
Quantity
16 units
Official record key
device-enforcement:Z-2540-2018

Official wording

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

Code information: Lot Numbers - 29147, 29148 & 29778

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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