Arrow recalls FlexTip Plus Epidural Catheterization Kits with potential LOR syringe failures causing dural puncture and blood patches. Affected kits have specific product codes and lots.
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 have LOR syringes failing, leading to dural puncture and possible blood patches. This could cause serious complications during epidural procedures.
The LOR syringes in the kit can fail, causing the needle to puncture the dura (protective layer around the spinal cord). This may require a blood patch to seal the leak, which can lead to serious complications like infection or neurological issues.
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 incorrectly.
Check for product code ASK-05503-BID on the kit. Affected lots include 23F19G0306, 23F19H0035, and 23F19K0149, 23F19L0411. The kit was sold by Arrow International Inc.
Look for the lot numbers 23F19G0306, 23F19H0035, 23F19K0149, or 23F19L0411 on the FlexTip Plus Epidural Catheterization Kit.
The LOR syringes in the kit can fail, causing dural puncture and potentially requiring a blood patch to seal the leak.
Check the lot number on the kit. If it matches the affected lots (23F19G0306, 23F19H0035, 23F19K0149, 23F19L0411), contact Arrow for guidance.
The recall record does not specify a remedy or fix for the LOR syringe failures.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1182-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1182-2020 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.
