Arrow recalls FlexTip Plus Epidural Catheterization Kit (ASK-02220-SRH) due to potential LOR syringe failures causing dural puncture and blood patches. Affected lots: 13F19F0303, 13F1:9G0072, 13F19L0140.
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Arrow is recalling FlexTip Plus Epidural Catheterization Kits with specific product codes because the LOR syringes might fail, leading to dural puncture and requiring blood patches. This could cause serious complications during epidural procedures.
The LOR syringes in the kit can fail during use, potentially causing dural puncture (a hole in the protective layer around the spinal cord). This may require a blood patch to seal the leak, which can lead to complications like infection or neurological issues.
Medical professionals who use the FlexTip Plus Epidural Catheterization Kit for epidural procedures are most at risk. Patients receiving epidural anesthesia may also be affected if the kit is used incorrectly.
Check for the product code ASK-02220-SRH on the kit. Affected lots include 13F19F0303, 13F19G0072, and 13F19L0140. The kit is sold by Arrow International Inc.
Look for the product code ASK-02220-SRH and affected lots: 13F19F0303, 13F19G0072, 13F19L0140.
The LOR syringes in the kit can fail, potentially causing dural puncture and requiring a blood patch.
Check the product code and lot numbers to see if it's affected. If it is, contact Arrow for guidance.
Yes, dural puncture can cause complications like infection or neurological issues, but the remedy is not specified in the recall.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1174-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1174-2020 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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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.
