Arrow Pediatric Catheter Kit Recall: Incorrect Labeling Risk

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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 pediatric catheter kits that are incorrectly labeled as a longer catheter than they actually are. This could lead to improper use in medical procedures, though no injuries have been reported.

Why it’s dangerous

The kit is labeled as containing an 8 cm catheter but actually has a 5 cm catheter. This size difference could cause improper insertion in infants, potentially leading to complications during medical procedures.

Who’s affected

Healthcare providers using pediatric catheter kits with product code AK-22502 are likely affected. Infants under specific weight thresholds may be at higher risk due to potential mismatch in catheter size.

How to tell if you have this one

Check for product code AK-22502 on the kit. The kit is labeled as a 2-lumen, 5 Fr x 8 cm catheter but contains a 2-lumen, 5 Fr x 5 cm catheter.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Code
Look for the product code AK-22502 on the kit to confirm if it is affected.

✎ GovInfoNow

Questions people ask

Is this recall causing any injuries?

No patient injuries have been reported related to this issue.

What is the correct catheter length?

The kit contains a 5 cm catheter, but is incorrectly labeled as an 8 cm catheter.

How can I tell if I have the affected product?

Check for product code AK-22502 on the kit.

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-2886-2018 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-2886-2018 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-2886-2018 (July 3, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2886-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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 Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502

Lower-risk recall