Intraosseous Needle Set Recall: Becton Dickinson Removes Certain Intraosseous Vascular Access System Needle Sets
Recall Summary Becton Dickinson is recalling certain BD Intraosseous Vascular Access System Needle Sets because the obturator (the inner stylet) can be difficult to remove after the needle is placed in a patient. This recall affects healthcare facilities and providers who use these specific needle sets for vascular access procedures.
- Recalling firm
- Intraosseous Needle Set
- Reason
- BD is recalling certain BD Intraosseous Vascular Access System Needle Sets due to difficulty removing the obturator (stylet) following placement.
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-08-17
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/62898ec9-00cf-4897-bfaf-0376ebffe9b2