Arrow recalls EPIDURAL CATHETERIZATION KIT (Product Code UR-05501-EXP) due to potential dural puncture from LOR syringes. Affected lots include 71F19B0757 through 71F19K1689. Consumers should contact Arrow for details.
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 EPIDURAL CATHETERIZATION KITS with Product Code UR-05501-EXP because the LOR syringes may cause dural puncture, which can require a blood patch. This risk affects medical professionals using the kits for epidural procedures.
The LOR syringes in the kits can fail, causing dural puncture (a tear in the protective membrane around the spinal cord). This may require a blood patch to seal the tear and prevent complications.
Medical professionals who use the recalled EPIDURAL CATHETERIZATION KITS for epidural procedures are most at risk. Patients receiving these procedures may also be affected if the kit is used incorrectly.
Check the Product Code UR-05501-EXP on the kit. Affected lots are listed as 71F19B0757, 71F19D1493, 71F19E2344, 71F19G2640, 71F19J0575, 71F19C0748, 71F19E0193, 71F19G1146, 71F19H2120, and 71F19K1689.
Look for Product Code UR-05501-EXP on the kit to confirm if it is affected.
The LOR syringes in the kits can fail, causing dural puncture which may require a blood patch.
Check the Product Code UR-05501-EXP and affected lots. Contact Arrow for instructions on next steps.
Yes, dural puncture can occur, which may require a blood patch to prevent complications.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1215-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1215-2020 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.
