Arrow FlexTip Plus Spinal Epidural Kit: Risk of Dural Puncture

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 spinal epidural kits because their LOR syringes might fail, causing dural puncture that could require a blood patch. This is a serious risk for medical procedures.

Why it’s dangerous

The LOR syringes in the kits can fail during use, potentially causing dural puncture. This means the spinal membrane could be accidentally pierced, requiring a blood patch to seal the leak.

Who’s affected

Healthcare professionals using the FlexTip Plus spinal epidural kits are most at risk. Patients undergoing spinal epidural procedures may also be affected.

How to tell if you have this one

Check for product code AA-05400-B on the kit. Affected lots include 71F19E2457, 71F19G0988, 71F19H1281, 71F19K2009, 71F19F1658, 71F19G2371, and 71F19J1079.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Code
Look for product code AA-05400-B on the kit packaging.
Contact Manufacturer
Contact Arrow International for specific guidance on the affected lots.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The LOR syringes in the kits can fail, potentially causing dural puncture that may require a blood patch.

What is the risk of using this product?

There is a potential for dural puncture, which could require a blood patch to seal the leak.

How can I check if I have the recalled product?

Check for product code AA-05400-B and affected lots listed in the recall notice.

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-1170-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1170-2020 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-1170-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1170-2020 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 Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B

Use caution until it’s fixed