Arrow recalls FlexTip Plus Epidural Catheterization Kits with potential for dural puncture due to LOR syringe failures. Affected kits may require blood patches. Stop using if you have the product code.
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 that may cause dural puncture (a hole in the spinal membrane) due to LOR syringe failures. This could lead to needing a blood patch to seal the hole. If you have the recalled product, stop using it immediately.
The LOR syringes in the kit can fail, causing a hole in the spinal membrane (dural puncture). This may require a blood patch to seal the hole and prevent complications like infection or nerve damage.
Healthcare professionals who use the FlexTip Plus Epidural Catheterization Kit for spinal procedures are most at risk. Patients receiving epidural anesthesia may also be affected if the kit is used improperly.
Check for product code JC-05400-E on the kit. Affected lots include 71F19A1623, 71F19B0507, 14F19D0467, and other specific lot numbers listed in the recall notice.
Immediately stop using the FlexTip Plus Epidural Catheterization Kit if you have the recalled product code.
The LOR syringes in the kit can fail, causing dural puncture which may require a blood patch to seal the hole.
Stop using the kit immediately and contact Arrow for further instructions.
Yes, affected lots include 71F19A1623, 71F19B0507, 14F19D0467, and other specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1203-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1203-2020 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.
