Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Harvest Graft Delivery System Recalled by Harvest Technologies Corporation Due to Potential for leur connector to leak or have...
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 Harvest Technologies Corporation directly.
Affected Products
Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft Delivery System is intended for the aspiration of bone marrow, autologous blood, plasma, or other body fluids. The system is indicated for die delivery of allograft, autograft, or synthetic bone graft materials to an orthopedic surgical site. In addition, it is designed to facilitate pre-mixing of bone graft materials with the aspirate(s), I.V. fluids, blood, plasma, platelet rich plasma, bone marrow or other specific blood component(s) as deemed necessary by the clinical use requirements.
Quantity: 730 cases (3 kits per case)
Why Was This Recalled?
Potential for leur connector to leak or have cracks.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Harvest Technologies Corporation
Harvest Technologies Corporation 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