Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Reflection Interfit Shell Recalled by Smith & Nephew Inc Due to Inner spherical radius of the shell is undersized.
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
Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection.
Quantity: 10 units
Why Was This Recalled?
Inner spherical radius of the shell is undersized.
Where Was This Sold?
This product was distributed to 2 states: FL, NJ
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