Arrow SnapLock Catheter/Syringe Adapter Recall: Unsealed Packaging Risk

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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 SnapLock Catheter/Syringe Adapters that may have unsealed packaging, risking contamination. This could lead to infections if the device is used without proper sterility.

Why it’s dangerous

The unsealed packaging could allow contaminants to enter the device, potentially causing infections if the adapter is used without proper sterility. This risk is present if the packaging is not sealed properly during manufacturing or shipping.

Who’s affected

Healthcare professionals and patients using the SnapLock adapters with unsealed packaging. Those most at risk are individuals who have the specific lot numbers listed in the recall.

How to tell if you have this one

Check the product code AS-05500 on the adapter. Affected units include lot numbers 13F17A0065, 13F17B0190, 13F17D0264, 13F17F0246, 13F17F0653, 13F17J0082, and 13F17K0412.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Code
Look for product code AS-05500 on the adapter to determine if it is affected.

✎ GovInfoNow

Questions people ask

What is the specific hazard with these adapters?

The unsealed packaging may allow contaminants to enter the device, potentially causing infections if used without proper sterility.

How can I tell if my adapter is affected?

Check the product code AS-05500 and lot numbers 13F17A0065, 13F17B0190, 13F17D0264, 13F17F0246, 13F17F0653, 13F17J0082, or 13F17K0412.

Do I need to stop using these adapters?

The recall does not specify a stop-use action; affected units should be checked for the product code and lot numbers.

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-1962-2018 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1962-2018 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-1962-2018 (April 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1962-2018 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 SnapLock" Catheter/Syringe Adapter; Product Code: AS-05500

Lower-risk recall