Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 Recalled by Biomet UK Ltd. Due to HipLOC System Plate Barrel due to an undersized...
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 Biomet UK Ltd. directly.
Affected Products
HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-130-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures
Quantity: 1 unit
Why Was This Recalled?
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Biomet UK Ltd.
Biomet UK Ltd. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report