Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Microseal Augmented (20 degrees) Liner Recalled by Signal Medical Corporation Due to Incorrect dimension on four liners was detected
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 Signal Medical Corporation directly.
Affected Products
Microseal Augmented (20 degrees) Liner, acetabular liner component made from UHMW polyethylene (ASTM F648). Sizes 36x52x20; and 36x50x20. Device is intended for use with Whiteside Biomechanics, Inc./Signal Medical Corporation Micro-Seal Shell in an uncemented Total Hip Replacement.
Quantity: 12 devices
Why Was This Recalled?
Incorrect dimension on four liners was detected
Where Was This Sold?
This product was distributed to 1 state: MO
About Signal Medical Corporation
Signal Medical Corporation 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