Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing Recalled by Synthes USA HQ, Inc. Due to The Synthes 4.5 mm LCP Curved Condylar Plate...
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 Synthes USA HQ, Inc. directly.
Affected Products
Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.
Quantity: 13
Why Was This Recalled?
The Synthes 4.5 mm LCP Curved Condylar Plate was recalled because a Straight Condylar Plate is etched with a Curved Condylar Plate part number.
Where Was This Sold?
This product was distributed to 5 states: FL, ID, LA, NY, TN
About Synthes USA HQ, Inc.
Synthes USA HQ, Inc. has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report