Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
R3 (TM) XLPE ACETABULAR LINER UHMWPE Recalled by Smith & Nephew Inc Due to One batch of 60 mm 20o R3 XLPE...
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 Smith & Nephew Inc directly.
Affected Products
R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD, QTY: (1), STERILE H2O2, REF 71335762. Orthopaedic.
Quantity: 53 units
Why Was This Recalled?
One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a 62 mm 20o liner and one batch of 62 mm 20o R3 XLPE liner may be laser etched and packaged as a 60 mm 20o liner.
Where Was This Sold?
This product was distributed to 13 states: FL, IN, IA, KY, MI, MO, NY, OR, PA, TN, TX, WA, WI
About Smith & Nephew Inc
Smith & Nephew Inc has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report