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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...

Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured

ARROW INTERNATIONALHealth & Personal CareMedical DevicesProduct code: ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 Batch Number: 33F25J0347

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
March 11, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
March 11, 2026
Hazard Level
HIGH
Brand
ARROW INTERNATIONAL
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
ARROW INTERNATIONAL
Model numbers
Product code: ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 Batch Number: 33F25J0347
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    March 11, 2026

  2. Reported by FDA DEVICE

    April 29, 2026

  3. RecallRadar source check

    May 6, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact ARROW INTERNATIONAL, LLC or your healthcare provider for instructions. Notification method: Letter

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Full Description

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.. Reason: Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured. Classification: Class II. Quantity: 85. Distribution: U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Product code: ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 Batch Number: 33F25J0347
Affected States
ALL
Report Date
April 29, 2026
Recall Status
ACTIVE

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