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 its EPIDURAL CATHETERIZATION KIT (Product Code DE-05400D-BO) because LOR syringes in the kits may fail, leading to dural puncture and requiring blood patches. This risk affects medical professionals using the kit for epidural procedures.

Why it’s dangerous

The LOR syringes in the kit may fail during use, causing dural puncture (a tear in the protective membrane around the spinal cord). This can lead to complications requiring blood patches to seal the leak.

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 DE-05400D-BO on the kit. Affected lots are 71F19D2769, 71F19H0716, and 71F19K1690. The kit is sold by Arrow International Inc.

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 71F19D2769, 71F19H0716, or 71F19K1690 on the kit packaging.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

The LOR syringes in the kit may fail, causing dural puncture and requiring blood patches.

What should I do if I have this kit?

Check the lot number on the kit. If it matches the affected lots (71F19D2769, 71F19H0716, 71F19K1690), contact Arrow for guidance.

Is there a fix for this issue?

The recall record does not specify a fix or 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-1195-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1195-2020 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-1195-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1195-2020 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 DE-05400D-BO

Use caution until it’s fixed