Arrow FlexTip Plus Spinal 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 spinal epidural kits that may cause dural puncture due to LOR syringes failing. This could require a blood patch and poses a risk during medical procedures.

Why it’s dangerous

The LOR syringes in the kits can fail, leading to dural puncture. This may cause a leak of cerebrospinal fluid and sometimes require a blood patch to seal the hole.

Who’s affected

Medical professionals using the FlexTip Plus kits for spinal epidural procedures are most at risk. Patients receiving these procedures may also be affected if the kit is used.

How to tell if you have this one

Check for product code ASK-05500-BID on the kit. Affected lots are 23F19E0337, 23F19J0065, 23F19K0100, 23F19L0218, 23F19H0048, 23F19J0314, 23F19K0303, and 23F19M0007.

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 ASK-05500-BID and affected lot numbers on the kit packaging.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

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

What should I do if I have this kit?

Check the product code and lot numbers to see if it's affected. If it is, contact Arrow for guidance.

Is there a fix for this issue?

The recall record does not specify a remedy or fix.

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-1178-2020 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1178-2020 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-1178-2020 (January 15, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1178-2020 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 Kit, Product Code ASK-05500-BID

Use caution until it’s fixed