Arrow CVC 2 Lumen Pediatric Set: Incorrect Priming Volume Hazard

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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 central venous catheter sets that have incorrect priming volume and flow rates as stated on the lidstock. This could lead to improper use during medical procedures if the device is used without correction.

Why it’s dangerous

The lidstock provides incorrect priming volume and flow rates, which could lead to improper use during medical procedures. This might cause complications if the device is used without adjusting for the errors.

Who’s affected

Healthcare providers using the Arrow CVC 2 Lumen Pediatric Set for short-term central venous access. Patients receiving treatments like chemotherapy or blood transfusions are at risk if the device is used incorrectly.

How to tell if you have this one

Check for the product name 'Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm'. Affected units are in lots 14F18F0336 and 14F18E0121.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot
Identify the lot number on the product packaging; affected lots are 14F18F0336 and 14F18E0121.

✎ GovInfoNow

Questions people ask

What is the hazard with this product?

The lidstock states the incorrect priming volume and flow rates, which could lead to improper use during medical procedures.

How can I tell if I have the recalled product?

Check for the product name 'Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm' and lot numbers 14F18F0336 or 14F18E0121.

What should I do if I have the recalled product?

The recall does not specify a remedy; contact Arrow directly for instructions.

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-0723-2019 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0723-2019 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-0723-2019 (November 14, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0723-2019 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 CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm,

Lower-risk recall