Official recall notice

FDA DeviceN/A

Intraosseous Vascular Access System Needle Sets Recall (Aug 2026)

Product: Intraosseous Vascular Access System Needle Sets

Recall date
2026-08-03
Brand
BD

Why it was recalled

Hazard

Due to Reports of Difficulty Removing the Obturator

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Product description

Due to Reports of Difficulty Removing the Obturator

Verify with the official notice →
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