BD Issues Nationwide Recall for Specific Lots of BD Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
August 04, 2026
August 04, 2026
WASHINGTON, Aug. 4 -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following recall notice:
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BD Issues Nationwide Recall for Specific Lots of BD(R) Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
Summary
Company Announcement Date: July 30, 2026
FDA Publish Date: August 03, 2026
Product Type: Medical Devices
. . .
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BD Issues Nationwide Recall for Specific Lots of BD(R) Intraosseous Vascular Access System Needle Sets Due to Reports of Difficulty Removing the Obturator
Summary
Company Announcement Date: July 30, 2026
FDA Publish Date: August 03, 2026
Product Type: Medical Devices
. . .