Arrow recalls echogenic introducer needles with specific UDI code due to incorrect adhesive manufacturing. Affected units may have safety risks; contact Arrow for details.
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
Arrow is recalling echogenic introducer needles with a specific UDI code because the liquid adhesive was incorrectly manufactured. This could lead to safety issues if the needle is used improperly.
The liquid adhesive was incorrectly manufactured, which could affect the needle's performance or safety during medical procedures. However, the exact risk is not specified in the recall notice.
Medical professionals using the Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 with the UDI code (01)10801902220315(17)261231(11)251210(10)33F25J0347 are most at risk.
Check for the UDI code (01)10801902220315(17)261231(11)251210(10)33F25J0347 on the needle packaging or product. The product code is ASK-04001-BWK2.
Verify the UDI code and product code on the needle to confirm if it is affected.
The recall is due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured.
Check for the UDI code (01)10801902220315(17)261231(11)251210(10)33F25J0347 on the needle packaging or product.
The recall notice does not specify a remedy, so contact Arrow directly for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1910-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1910-2026 from Arrow. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
