BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
- Date
- Jul 30, 2026
- Company
- (Becton, Dickinson and Company)
- Brand
- BD
- Product
- Intraosseous Vascular Access System Needle Sets
- Reason
- Due to Reports of Difficulty Removing the Obturator
- Hazard
- Other
- Source
- FDA
How to identify the product
- The affected lots were manufactured with out of tolerance dimensions and distributed between September 30, 2024, and June 12, 2026.
- BD will issue replacement for destroyed product of the affected lot numbers to customers that purchased the affected product directly from BD, following receipt of the completed Customer Response Form.
- Product distributed outside of the affected production window is not impacted.
Facts are taken from the official notice. If anything here differs from it, the official notice is correct.