Stelkast Co: Medical Device Recall in 2013 - (Recall #: Z-1066-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Stelkast Cross-over Acetabular Shell and Liner Hip System, Part Numbers SC3458-52, SC3474-52, SC3459-52, and SC3460-52. Intended for use in reconstruction of the articulating surface of the acetabular portion of the hip.

Product Classification:

Class II

Date Initiated: January 24, 2013

Date Posted: April 17, 2013

Recall Number: Z-1066-2013

Event ID: 64505

Reason for Recall:

Firm was made aware of incidents relating to the difficulty of properly engaging and securing the Cross-Over 36mm liner into the Cross-Over shell.

Status: Terminated

Product Quantity: 254

Code Information:

Part Numbers SC3458-52, lot number 28820-112612; SC3474-52, lot number 28822-101812; SC3459-52, lot number 28823-101812; and SC3460-52, lot number 28821-000.

Distribution Pattern:

Nationwide Distribution including the states of NV, OK and PA.

Voluntary or Mandated:

Voluntary: Firm initiated