Arrow recalls specific epidural catheterization kits (product code UR-05501) due to potential dural puncture from LOR syringes. Affected kits may require blood patches.
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 certain epidural catheterization kits because the LOR syringes inside can cause dural puncture, which may require a blood patch. This risk affects medical professionals using the kits for epidural procedures.
The LOR syringes in the kits can fail, causing the needle to puncture the dura mater (the protective layer around the spinal cord). This may lead to a spinal headache or require a blood patch to seal the leak.
Medical professionals who use the recalled epidural catheterization kits for procedures are most at risk. Patients receiving epidural anesthesia during these procedures could be affected if the kit is used.
Check for product code UR-05501 with lots: 71F19C0040, 71F19E1143, 71F19G1454, 71F19H2552, 71F19C1116, 71F19E2861, 71F19H0787, or 71F19J0868.
Identify the lot number on the kit packaging to confirm if it matches the listed lots: 71F19C0040, 71F19E1143, 71F19G1454, 71F19H2552, 71F19C1116, 71F19E2861, 71F19H0787, or 71F19J0868.
The LOR syringes can fail, causing dural puncture which may require a blood patch to treat the spinal leak.
No, but you should check the lot numbers to see if your kit is affected. If it is, take steps to avoid dural puncture.
The official recall notice does not specify how to obtain a blood patch; medical professionals should consult their healthcare provider.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1214-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1214-2020 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.
