Official recall record

BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF: D015251NK, BD Needle Kit

US FDA — Medical Devices · 2026-07-30 · United StatesClass I

Issuing authority: US FDA — Medical Devices
Alert date: 2026-07-30
Country of alert: United States
Alert level: Class I
Alert type: recall
Barcode (EAN/GTIN): 00801741163586
Brand on record: Bard Access Systems, Inc.

What the authority reported

After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-17.

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