Arrow EPIDURAL CATHETERIZATION KIT Recall: Risk of Dural Puncture

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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 EPIDURAL CATHETERIZATION KIT (Product Code AT-05501-LIN) because LOR syringes in the kits can fail, leading to dural puncture and possible blood patches. This risk affects medical professionals using the kit for epidural procedures.

Why it’s dangerous

The LOR syringes in the kit can fail during use, causing dural puncture (a tear in the protective membrane around the spinal cord). This may require a blood patch to seal the leak, which can be painful and risky for patients.

Who’s affected

Medical professionals who use the recalled EPIDURAL CATHETERIZATION KIT for epidural procedures are most at risk. Patients receiving epidural treatments with this kit could also be affected.

How to tell if you have this one

Check for the Product Code AT-05501-LIN on the kit. Affected lots are 71F19C1431, 71F19H1811, and 71F19K1515. The kit is sold for epidural procedures.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Lot Number
Look for the lot numbers 71F19C1431, 71F19H1811, or 71F19K1515 on the kit packaging.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

The LOR syringes in the kit can fail, causing dural puncture which may require a blood patch.

What should I do if I have this kit?

Check the lot number on the kit. If it matches the affected lots, stop using it and contact Arrow for instructions.

Is there a fix for this issue?

The recall record does not specify a remedy or fix.

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-1187-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1187-2020 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-1187-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1187-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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 EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN

Use caution until it’s fixed