Arrow Multi Lumen Catheter Kit Recall: Incorrect Springwire Guide Risk

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling Multi Lumen Central Venous Catheterization Kits that may contain an incorrect Springwire Guide (SWG). This could cause improper use during medical procedures, potentially leading to complications for patients.

Why it’s dangerous

The kits may contain the wrong Springwire Guide (SWG), which could lead to improper catheter placement during medical procedures. This might cause complications like infection or incorrect blood flow.

Who’s affected

Healthcare professionals using these kits for central venous catheterization procedures are most at risk. Patients receiving such procedures may also be affected if the kit is used incorrectly.

How to tell if you have this one

Check for product code ASK-12703-WMC1 and expiration dates between February 2018 and November 2018. Lot number 23F17C0757 is also associated with this recall.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the product code, expiration dates, and lot number to confirm if the kit is affected.

✎ GovInfoNow

Questions people ask

What is the product code for the recalled kits?

The product code is ASK-12703-WMC1.

What expiration dates are associated with the recalled kits?

The kits expire between February 2018 and November 2018.

What lot number is linked to this recall?

Lot number 23F17C0757.

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-0652-2018 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-0652-2018 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-0652-2018 (October 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0652-2018 to see it in context.
Plain-language summary written by qwen3:4b on September 14, 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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