Arrow FlexTip Plus Epidural 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 FlexTip Plus Epidural Catheterization Kits that may cause dural puncture due to LOR syringes failing. This could lead to requiring a blood patch to treat the puncture. If you have the recalled kits, stop using them immediately.

Why it’s dangerous

The LOR syringes in the kit can fail, causing the needle to puncture the dura (protective layer around the spinal cord). This may require a blood patch to seal the puncture site and prevent complications.

Who’s affected

Healthcare professionals using the FlexTip Plus Epidural Catheterization Kit for spinal procedures are most at risk. Patients receiving epidural anesthesia may also be affected if the kit is used incorrectly.

How to tell if you have this one

Check for the product code TI-05501-ME on the kit. Affected lots include 71F19A1324 through 71F19L0033. The kit is sold by Arrow International Inc.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Kit Now
Immediately stop using the FlexTip Plus Epidural Catheterization Kit if you have it.

✎ 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 is the product code for the recalled kit?

The product code is TI-05501-ME.

Which lots are affected?

Affected lots include 71F19A1324 through 71F19L0033.

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-1212-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1212-2020 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-1212-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1212-2020 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 TI-05501-ME

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