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 require a blood patch and poses a risk of serious complications during epidural procedures.

Why it’s dangerous

The LOR syringes in the kits can fail, leading to dural puncture. This may cause spinal fluid leakage and sometimes requires a blood patch to seal the leak.

Who’s affected

Healthcare professionals using the FlexTip Plus Epidural Catheterization Sets for epidural 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 on the packaging. Affected lots are 71F19B2081, 71F19C1655, 71F19E2128, 71F19G2444, 71F19B2586, 71F19E1245, 71F19F1432, and 71F19J1685.

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 on the packaging to identify if it's in the affected lots listed.

✎ GovInfoNow

Questions people ask

What is the risk of using this product?

The LOR syringes may fail, causing dural puncture which can require a blood patch and lead to serious complications.

How can I tell if I have the recalled product?

Check the product code on the packaging. Affected lots include 71F19B2081 through 71F19J1685.

What should I do if I have the recalled product?

The recall does not specify a remedy, so contact Arrow directly for guidance.

Take action

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We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.

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Subject: Recall Z-1171-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1171-2020 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-1171-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1171-2020 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 AA-05400-E

Use caution until it’s fixed