Arrow AGB+ Multi-Lumen CVC Kit Recall: Incorrect Length Labeling

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling its AGB+ Multi-Lumen CVC Kit (product code CDC-42703-1A) because the label incorrectly states the catheter length. This could lead to improper medical procedures if the catheter is too long for the intended use.

Why it’s dangerous

The kit's label incorrectly states the catheter length as 20cm when it is actually 16cm. This mismatch could lead to improper insertion or complications during medical procedures if the catheter is too long for the intended vein access.

Who’s affected

Healthcare professionals using the Arrow AGB+ Multi-Lumen CVC Kit for medical procedures are most at risk. Patients receiving the kit may be affected if the incorrect length causes complications.

How to tell if you have this one

Check for the product code CDC-42703-1A on the kit. The kit was sold with lot number 13F18L0759. The label should state a 16cm catheter length.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the product code CDC-42703-1A and verify the catheter length is 16cm.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

The kit's label incorrectly states the catheter length as 20cm when it is actually 16cm.

What is the correct catheter length?

The correct catheter length is 16cm, as stated on the banner card.

How can I check if I have the recalled kit?

Check for the product code CDC-42703-1A and lot number 13F18L0759 on the kit label.

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-0192-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0192-2020 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-0192-2020 (July 18, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0192-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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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