Arrow Central Venous Catheter Kit Recall: Unsealed Packaging Risks Infection

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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 central venous catheter kits that could have unsealed packaging, potentially allowing contamination. This could lead to infections if used for medical procedures.

Why it’s dangerous

The packaging may not be sealed properly, which could allow contamination. If the kit is used without sterile conditions, it might introduce infections into the patient's body.

Who’s affected

Healthcare professionals using the catheter kits for medical procedures are most at risk. Patients receiving these kits may also be affected if the sterility is compromised.

How to tell if you have this one

Check for the product code ASK-15402-HOP on the packaging. Lot numbers 13F17C0183 and 13F17F0775 are also associated with this recall.

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 tampering or unsealed condition.
Contact Manufacturer
Reach out to Arrow International for guidance on whether the kit is affected by this recall.

✎ GovInfoNow

Questions people ask

Is this recall affecting patients directly?

The recall is for healthcare professionals using the kits; patients are affected only if the kits are used without proper sterility.

How can I tell if my kit is recalled?

Look for product code ASK-15402-HOP and lot numbers 13F17C0183 or 13F17F0775 on the packaging.

Do I need to stop using the kit immediately?

The recall does not require immediate stop-use; healthcare professionals should check the packaging seal and contact Arrow for guidance.

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-1978-2018 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1978-2018 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-1978-2018 (April 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1978-2018 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.

Arrow International Inc recalls Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Code:

Lower-risk recall