BD Recalls Intraosseous Products

6/23/22 — BD (Becton, Dickinson and Company) announced a voluntary recall on the BD™ Intraosseous Needle Set Kits, BD™ Intraosseous Manual Driver Kits, and BD™ Intraosseous Powered Drivers. Manufacturing defects in these products may result in delays in care due to limited or non-functioning intraosseous access or could also lead to needlestick injuries. Affected needle kits should be destroyed in compliance with the healthcare institution’s process for disposal. Read the FDA recall notice.