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 specific epidural catheterization kits that may cause dural puncture (a hole in the spinal membrane) due to failures in the LOR syringes. This could require a blood patch to treat the injury.

Why it’s dangerous

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

Who’s affected

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

How to tell if you have this one

Check the product code on the kit: MTO-09903-KU. Look for lot numbers 71F19B1406, 71F19E2026, or 71F19G1921. These kits were sold by Arrow International Inc.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Code
Verify the product code is MTO-09903-KU to confirm if the kit is recalled.
Contact Manufacturer
Reach out to Arrow International Inc. for guidance on next steps if the kit is recalled.

✎ 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.

What should I do if I have this kit?

Check the product code and lot numbers to see if it's recalled. Contact Arrow International Inc. for further instructions.

Is there a risk of serious injury?

Yes, dural puncture can occur, which may require a blood patch to treat the injury.

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-1210-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1210-2020 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-1210-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1210-2020 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 MTO-09903-KU

Use caution until it’s fixed