Arrow 8Fr Catheter Clamp Recall: Unsealed Packaging Risks Infection

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling 8Fr Catheter Clamps with Fastener (Product Code CC-00008) because the packaging may not be sealed properly, potentially allowing contamination. This could lead to infections if the device is used without proper sterility.

Why it’s dangerous

The catheter clamps' packaging may not be sealed properly, which could allow contamination. If the device is used without proper sterility, it might lead to infections.

Who’s affected

Healthcare professionals and patients using the 8Fr Catheter Clamps with Fastener (Product Code CC-00008) are affected. Those who have the specific lot numbers listed are most at risk.

How to tell if you have this one

Check for the Product Code CC-00008 on the packaging. Affected units include lot numbers 13F17B0050, 13F17D0271, 13F17F0078, and 13F17J0276.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Packaging
Look for the Product Code CC-00008 and the specific lot numbers listed.

✎ GovInfoNow

Questions people ask

Why is this catheter clamp being recalled?

The packaging may not be sealed properly, which could allow contamination and lead to infections if used without proper sterility.

What lot numbers are affected?

Lot numbers 13F17B0050, 13F17D0271, 13F17F0078, and 13F17J0276.

Is there a remedy for this recall?

The recall record does not specify a remedy.

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-2009-2018 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-2009-2018 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-2009-2018 (April 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2009-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 21, 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 8Fr. Catheter Clamp with Fastener; Product Code: CC-00008

Lower-risk recall