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 KITS with Product Code BE-05400-DCHH because the LOR syringes may cause dural puncture, requiring a blood patch in some cases. This risk affects medical professionals using the kits for epidural procedures.

Why it’s dangerous

The LOR syringes in the kits can fail, leading to dural puncture (a tear in the protective membrane around the spinal cord). This may require a blood patch to seal the leak, which can cause pain and complications.

Who’s affected

Medical professionals who use the recalled EPIDURAL CATHETERIZATION KITS for epidural procedures are most at risk. Patients receiving these procedures may also be affected if the kit is used incorrectly.

How to tell if you have this one

Check for Product Code BE-05400-DCHH on the kit. Affected lots are 71F19D0610 and 71F19G2151. The recall applies to kits sold with these specific lot numbers.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Lot Number
Look for lot numbers 71F19D0610 or 71F19G2151 on the EPIDURAL CATHETERIZATION KIT packaging.

✎ GovInfoNow

Questions people ask

What is the risk of using this kit?

The LOR syringes may cause dural puncture, which can require a blood patch to seal the leak and may cause pain or complications.

Do I need to stop using this kit immediately?

No, but you should check the lot number to see if your kit is affected. If it is, contact Arrow for guidance.

How can I get a replacement kit?

The recall record does not specify a replacement process. Contact Arrow directly for assistance.

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-1189-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1189-2020 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-1189-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1189-2020 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 BE-05400-DCHH

Use caution until it’s fixed