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 syringes failing. This could lead to serious complications requiring blood patches. Affected units have specific lot numbers listed in the recall.

Why it’s dangerous

The LOR syringes in the kits can fail, causing dural puncture. This may require a blood patch to seal the leak. The failure risk is higher during spinal procedures where precise placement is critical.

Who’s affected

Medical professionals using the FlexTip Plus Epidural Catheterization Sets for spinal procedures are most at risk. Patients receiving epidural anesthesia may also be affected if the device fails.

How to tell if you have this one

Check the product code JC-05400-DCS on the packaging. Affected lots include 71F19B0226 through 71F19H2404. The recall covers specific batches sold to medical facilities.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for the lot numbers listed in the recall: 71F19B0226 to 71F19H2404.
Contact Arrow for Details
Reach out to Arrow International Inc. for specific instructions on next steps.

✎ GovInfoNow

Questions people ask

What is the risk of using this product?

The LOR syringes may fail, causing dural puncture which could require a blood patch to treat.

How can I tell if I have the recalled product?

Check the product code JC-05400-DCS and lot numbers 71F19B0226 through 71F19H2404.

Do I need to stop using the product immediately?

The recall does not require immediate stop use; medical professionals should follow Arrow's instructions.

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-1202-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1202-2020 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-1202-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1202-2020 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 JC-05400-DCS

Use caution until it’s fixed