Arrow EPIDURAL CATHETER KIT Recall: Risk of Dural Puncture from LOR Syringes

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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 certain epidural catheterization kits because the LOR syringes inside can fail, leading to dural puncture and possible need for blood patches. This risk affects medical professionals using the kits for spinal procedures.

Why it’s dangerous

The LOR syringes in the kits can fail during use, causing dural puncture (a hole in the spinal membrane). This may require a blood patch to seal the hole and prevent complications.

Who’s affected

Medical professionals who use the recalled epidural catheterization kits for spinal 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 the Product Code BE-080180-BXL on the kit. Affected lots include 71F19B0729, 71F19E2327, 71F19G1496, 71F19J1005, 71F19C1089, 71F19F0733, and 71F19H0793.

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 listed: 71F19B0729, 71F19E2327, 71F19G1496, 71F19J1005, 71F19C1089, 71F19F0733, or 71F19H0793.
Contact Manufacturer
Reach out to Arrow International for guidance on next steps if the kit is affected.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

The LOR syringes in the kits can fail, causing dural puncture which may require a blood patch to seal the hole.

What should I do if I have this kit?

Check the lot number on the kit. If it matches the affected lots, contact Arrow International for guidance.

Is there a risk of serious injury?

Yes, dural puncture can occur, which may require a blood patch to prevent complications.

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-1191-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1191-2020 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-1191-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1191-2020 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-080180-BXL

Use caution until it’s fixed