Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to Mislabeling
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 Blue Belt Technologies MN directly.
Affected Products
Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral. Unicondylar Knee prosthesis.
Quantity: 2
Why Was This Recalled?
Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains PFSI-00054, Right Medial/Left lateral implants. Packages labeled PFSI-00054, Stride Right Medial/Left Lateral contain PFSI-00053, Left Medial/Right Lateral.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Blue Belt Technologies MN
Blue Belt Technologies MN has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report