Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ulnar Osteotomy Compression Plate Recalled by TriMed Inc. Due to Two instrument holes located on the side of...
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
Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed Ulnar Osteotomy Plate is intended for use in osteotomy procedures of the ulna.
Quantity: 722
Why Was This Recalled?
Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate
Where Was This Sold?
This product was distributed to 1 state: TX
About TriMed Inc.
TriMed Inc. has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report