Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
POLARSTEM COLLAR Reamer Guide Recalled by Smith & Nephew Orthopaedics AG Due to Multiple lots being recalled due to a product...
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 Orthopaedics AG directly.
Affected Products
POLARSTEM COLLAR Reamer Guide, Catalog Number: 75102205, UPC Codes: 00885556535493 - Product Usage: Once the appropriate trial rasp size is in place, the adapter is removed and the calcar reamer guide (75102205) is positioned on the rasp. The calcar reamer (75102207 or 75102208) is placed over the reamer guide and the femoral neck is machined until the reamer reach the physical stop-fully seated on the inner reamer guide.
Quantity: 528 unit
Why Was This Recalled?
Multiple lots being recalled due to a product design issue
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Smith & Nephew Orthopaedics AG
Smith & Nephew Orthopaedics AG has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report