Arrow FlexTip Plus Epidural Catheter Set 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 Sets that may cause dural puncture due to LOR syringe failures. This could lead to needing a blood patch to treat the puncture. Patients using these sets should stop using them and contact Arrow for a replacement.

Why it’s dangerous

The LOR syringes in the kits can fail, causing dural puncture. 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 Sets for spinal procedures are most at risk. Patients receiving epidural anesthesia through these sets may also be affected.

How to tell if you have this one

Check the product code on the packaging: MP-17019-TIP. Affected lots include 13F19A0544, 13F19B0451, 13F19E0017, 13F19K0394, 13F19A0796, 13F19D0481, 13F19G0086, and 13F19L0070.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using the Set
Immediately stop using the FlexTip Plus Epidural Catheterization Set if it has the affected product codes listed.

✎ GovInfoNow

Questions people ask

What is the specific hazard with these catheters?

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

Which lots are affected?

Affected lots include 13F19A0544, 13F19B0451, 13F19E0017, 13F19K0394, 13F19A0796, 13F19D0481, 13F19G0086, and 13F19L0070.

How can I get a replacement?

Contact Arrow directly for a replacement or refund.

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-1206-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1206-2020 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-1206-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1206-2020 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 Set, Product Code MP-17019-TIP

Use caution until it’s fixed