Notice names this product. ARROW INTERNATIONAL’s Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code is named in FDA Class II recall Z-1910-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured Identifying details: Product code: ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 Batch Number: 33F25J0347. Units affected: 85. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is intended for injection or aspiration of fluids. The needle protection device covers the needle after use to help prevent needle sticks.
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code recall status
Official ID Z-1910-2026 · Official record ↗
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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.