Arrow PICC Kits May Have Wrong Length Stylet - Risk of Incorrect Use

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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 PICC kits that may contain the wrong stylet length (40cm instead of : 50cm or vice versa). Using the incorrect length could cause improper use of the catheter, potentially leading to complications.

Why it’s dangerous

The kits may contain a 40cm stylet when labeled as 50cm or a 50cm stylet when labeled as 40cm. Using the wrong length could lead to improper catheter placement, potentially causing complications.

Who’s affected

Healthcare professionals using Arrow PICC kits with product code CDC-45052-VPS2 are affected. Patients receiving these kits may be at risk if the incorrect stylet length causes improper catheter placement.

How to tell if you have this one

Check for product code CDC-45052-VPS2 on the kit. Kits labeled as containing a 40cm PICC may have a 50cm stylet, and vice versa.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Label
Look for product code CDC-45052-VPS2 on the kit label to confirm it's affected.

✎ GovInfoNow

Questions people ask

What is the product code for the affected kits?

The product code is CDC-45052-VPS2.

Why is this recall happening?

The kits may contain a 40cm stylet when labeled as 50cm or a 50cm stylet when labeled as 40cm, which could lead to improper catheter placement.

What should I do if I have the affected kit?

The recall record does not specify a remedy, so check with Arrow International 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-1365-2019 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1365-2019 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-1365-2019 (December 13, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1365-2019 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 Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-45052-VPS2 Product Usage: The Arrow Pressure

Lower-risk recall