• BD launched a voluntary nationwide recall to the user level for specific lots of BD Intraosseous Vascular Access System needle sets.
• Recall follows reports of difficulty removing the obturator after placement, potentially forcing new access attempts and delaying urgent treatment.
• BD reported 75 complaints through June 2026, including 45 serious injuries plus 4 deaths tied to resuscitation efforts in out-of-hospital cardiac arrests.
• Affected lots were distributed from Sept. 30, 2024 to June 12, 2026; the BD Intraosseous Powered Driver is not included.
• Customers were told to stop using affected lots and destroy inventory; BD plans to replace destroyed product for direct purchasers.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. BD - Becton, Dickinson and Company published the original content used to generate this news brief on July 31, 2026, and is solely responsible for the information contained therein.