Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TriMed Semi-Tubular Plate Recalled by Trimed Inc Due to TriMed is recalling the Semi-Tubular Plates with 10...
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 Trimed Inc directly.
Affected Products
TriMed Semi-Tubular Plate, 10-Hole, Model No. SMTP-10 Contoured plate with offset screw holes. The plate is 103 mm in length, 1.3 mm thick and 9.6 mm wide. The part is made of surgical steel conformance with ASTM F138 or F139. The plate is used to fixation of long bone fractures. The TriMed Bone Plates are intended for use in the fixation of fractures to the Tibia, Fibula, Ulna, Radius and the Humerus.
Quantity: 30 units
Why Was This Recalled?
TriMed is recalling the Semi-Tubular Plates with 10 holes (SMTP-10) because a non-locking screw passed through a hole in a SMTP-10 plate being implanted.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Trimed Inc
Trimed Inc 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