Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Recalled by Trilliant Surgical Ltd. Due to The cutting efficiency of the Countersinks was out...
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 Trilliant Surgical Ltd. directly.
Affected Products
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part # 210-40-002 NON-STERILE Product Usage: The Tiger Cannulated Screw Fixation System implants are intended for fixation of fractures, non-unions, arthrodesis, and osteotomies of the small bones in the hand and foot. The implants and guide wires are intended for single use only.
Quantity: 102 units
Why Was This Recalled?
The cutting efficiency of the Countersinks was out of specification.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Trilliant Surgical Ltd.
Trilliant Surgical Ltd. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report