Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM Recalled by Synthes, Inc. Due to The 10 mm/135 degree Titanium Cannulated Trochanteric Fixation...
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, Inc. directly.
Affected Products
10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM - Sterile: intended to treat stable and unstable fractures of the proximal femur
Quantity: 6
Why Was This Recalled?
The 10 mm/135 degree Titanium Cannulated Trochanteric Fixation Nail 170 MM (Sterile) was assembled incorrectly. If the non conformance goes undetected, it may impact the locking function post-operatively and compromise the bone reduction and construct stability which may lead to non-union/malunion.
Where Was This Sold?
This product was distributed to 5 states: AK, FL, OH, OK, TX
About Synthes, Inc.
Synthes, Inc. has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report