Arrow recalls FlexTip Plus Epidural Catheterization Sets with potential for LOR syringe failures causing dural puncture and blood patches. Affected units include 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 Sets that may cause dural puncture due to LOR syringe failures. This could require a blood patch and poses a risk of serious injury during epidural procedures.
The LOR (loss of resistance) syringes in the kits can fail, leading to accidental puncture of the dura mater (the protective layer around the spinal cord). This may require a blood patch to seal the leak and could cause serious complications during epidural procedures.
Healthcare professionals using the FlexTip Plus Epidural Catheterization Sets for epidural procedures are most at risk. Patients receiving epidural anesthesia may also be affected if the device fails.
Check for product code JC-05400-B on the packaging. Affected units include specific lots listed in the recall notice, such as 71F19A0552 through 71F19J2204.
Verify the product code and lot numbers on the packaging to confirm if your device is affected.
Reach out to Arrow International for guidance on next steps if your device is recalled.
The LOR syringes may fail, causing dural puncture which could require a blood patch and pose serious injury risks during epidural procedures.
Check for product code JC-05400-B and specific lot numbers listed in the recall notice, such as 71F19A0552 through 71F19J2204.
Contact Arrow International for guidance on next steps, as the recall does not include a specific remedy.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1201-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1201-2020 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.
