BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
USBD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
Product Description & Identification
FRANKLIN LAKES, N.J. (July 31, 2026) – BD (Becton, Dickinson and Company) is voluntarily recalling specific lots of BD® Intraosseous Vascular Access System Needle Sets to the user level. These products are being recalled following reports that some users experienced difficulty removing the obturato
Additional Source Details
| Field | Value |
|---|---|
| Guid › #text | http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-nationwide-recall-specific-lots-bdr-intraosseous-vascular-access-system-needle-sets-due |
| Guid › @ is Perma Link | true |
| Link | http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-issues-nationwide-recall-specific-lots-bdr-intraosseous-vascular-access-system-needle-sets-due |
| Pub Date | Thu, 30 Jul 2026 18:01:00 EDT |
| Dc:creator | FDA |
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🚨 SAFETY ALERT: BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator Check if your household is affected: https://therecallfile.com/recalls/bd-issues-nationwide-recall-for-specific-lots-of-bd-intraosseous-vascu/RSS-FDA-RSS-v132oz
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