Reported Aug 3, 2026 · Announced

(Becton, Dickinson and Company) recalls BD Intraosseous Vascular Access System Needle Sets due to Due to Reports of Difficulty Removing the Obturator

(Becton, Dickinson and Company)

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

What you should do

Stop using the product and follow the return or refund instructions in the firm's announcement.

Is this the product you have?

  • Intraosseous Vascular
  • Access System Needle Sets BrandBD. Medical Devices

Why it was recalled

Due to Reports of Difficulty Removing the Obturator

The agency has not ranked the risk yet — treat the notice as a caution.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration

Read the FDA (recalls & safety alerts) notice

Data as of Sep 19, 5:56 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.