Arrow Multi-Lumen Catheter Kit Recall: Unsealed Packaging Risks Contamination

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Recalling firmArrow International Inc2400 Bernville Rd, N/A · Reading, PA 19605-9607

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling certain Multi-Lumen Central Venous Catheterization Kits because the packaging might not be sealed properly. This could lead to contamination and infection if the kit is used without proper sterility.

Why it’s dangerous

The packaging may not be sealed correctly, which could allow contaminants to enter the kit. This might lead to infections if the kit is used without proper sterility checks.

Who’s affected

Healthcare professionals who use these kits for central venous catheterization are most at risk. Patients receiving treatments with these kits could also be affected if sterility is compromised.

How to tell if you have this one

Check for product codes ASK-45703-SCH, ASK-45703-UAB, or ASK-45703-VAH. Look for specific lot numbers listed in the recall notice.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Packaging Seal
Inspect the packaging for any signs of being unsealed or damaged.

✎ GovInfoNow

Questions people ask

What product codes are affected?

Product codes ASK-45703-SCH, ASK-45703-UAB, and ASK-45703-VAH are affected.

What lot numbers are included?

Lot numbers include 13F17B0193, 13F17E0461, 13F17G0450 for ASK-45703-SCH; 13F17C0210 for ASK-45703-UAB; and 13F16M0294, 13F17E0398, 13F17H0074 for ASK-45703-VAH.

Is there a remedy for this recall?

The recall record does not specify a remedy.

Take action

Contact Arrow

We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2004-2018 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-2004-2018 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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Where this comes from

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.

Official source: FDA Recall #Z-2004-2018 (April 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2004-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

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