Arrow recalls FlexTip Plus Epidural Catheterization Kits with potential LOR syringe failures causing dural puncture and blood patches. Affected lots: 13F19B0343, 13F19B0501, 13F19E0698, 13F19H0470.
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 because LOR syringes in some lots may fail, causing dural puncture and requiring blood patches. This could lead to serious complications if the syringes malfunction during epidural procedures.
The LOR syringes in the kit can fail during use, potentially puncturing the dura (the protective layer around the spinal cord). This may require a blood patch to seal the leak, which can cause complications like infection or nerve damage.
Healthcare professionals using 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 improperly.
Check the product code on the kit: ASK-05400-CA1. Affected lots are 13F19B0343, 13F19B0501, 13F19E0698, and 13F19H0470. The kit is sold for epidural anesthesia procedures.
Look for the lot numbers 13F19B0343, 13F19B0501, 13F19E0698, or 13F19H0470 on the product packaging.
The LOR syringes in some lots may fail during use, causing dural puncture and requiring a blood patch.
Check the lot number on the kit. If it matches the affected lots, stop using it and contact Arrow for guidance.
Yes, dural puncture can cause complications like infection or nerve damage, requiring a blood patch.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1179-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1179-2020 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.
