Official recall record

Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15192-VFI, CS-15192-VFI

US FDA — Medical Devices · 2026-04-10 · United StatesClass I

Issuing authority: US FDA — Medical Devices
Alert date: 2026-04-10
Country of alert: United States
Alert level: Class I
Alert type: recall
Barcode (EAN/GTIN): 10801902126709
Brand on record: ARROW INTERNATIONAL, LLC
Product category: Medical Device

What the authority reported

16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

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 2026-05-31.

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