Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by Stelkast Co Due to Firm was made aware of incidents relating to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stelkast Co directly.
Affected Products
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.
Quantity: 254
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stelkast Co
Stelkast Co has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report