Arrow FlexTip Plus Epidural Kit: Risk of Dural Puncture from LOR Syringes

Take action

Contact the company & request your remedy

Recalling firmArrow International Inc2400 Bernville Rd · Reading, PA 19605-9607

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling FlexTip Plus Epidural Catheterization Kits (product code ASK-05501-SH) because the LOR syringes in some kits can cause dural puncture, which may require a blood patch. This risk affects medical professionals using the kits for epidural procedures.

Why it’s dangerous

The LOR syringes in the kit can fail, leading to dural puncture (a hole in the protective membrane around the spinal cord). This may cause pain, infection, or require a blood patch to seal the leak.

Who’s affected

Medical professionals who use the FlexTip Plus Epidural Catheterization Kit for epidural procedures are most at risk. Patients receiving epidural anesthesia through this kit could experience complications.

How to tell if you have this one

Check for product code ASK-05501-SH on the kit. The affected lots are 23F19A0240, 23F19G0305, 23F19J0292, 23F19L0414, 23F19E0112, 23F19G0496, and 23F19K0152.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot
Look for the product code ASK-05501-SH and affected lots 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 product code and lot numbers. If affected, contact Arrow for guidance.

Is there a risk of serious injury?

Yes, dural puncture can cause pain, infection, or require a blood patch.

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-1180-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1180-2020 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-1180-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1180-2020 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 FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH

Use caution until it’s fixed