Harvest Technologies Corporation: Medical Device Recalls in 2013

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Harvest Technologies Corporation in 2013. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

2013

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.