Omnilife Science Inc.: Medical Device Recall in 2014 - (Recall #: Z-2241-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Apex Arc Hip Stem, Size 2, HA Coated; Product Code: HC-21002-HA

Product Classification:

Class II

Date Initiated: May 9, 2014

Date Posted: August 27, 2014

Recall Number: Z-2241-2014

Event ID: 68527

Reason for Recall:

Staining on hip implant.

Status: Terminated

Product Quantity: 13 devices

Code Information:

Lot: 17284

Distribution Pattern:

US: CA, OK, VA, FL, MA, NY, TX

Voluntary or Mandated:

Voluntary: Firm initiated