FDA MedWatch Safety AlertsOriginal article
BD Issues Nationwide Recall for Specific Lots of BD® Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
RegulatoryBD Intraosseous Vascular Access System Needle SetsNegative
AI Analysis
Summary
BD voluntarily recalls specific lots of BD Intraosseous Vascular Access System Needle Sets due to reports of difficulty removing the obturator. The recall is being issued to the user level following customer complaints.
Outcome Details
Voluntary nationwide recall of specific lots due to difficulty removing obturator
Importance:4/10
Sentiment:
-0.70
recallsafetymedical deviceregulatorypatient safety
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Published by FDA MedWatch Safety Alerts on August 3, 2026 4:00 AM