Arrow recalls FlexTip Plus Combined Spinal Epidural Catheterization Kits with potential for dural puncture due to LOR syringe failures. Affected lots include 13F18L0892 through 13F19L0079.
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 spinal epidural catheter kits that may cause dural puncture due to LOR syringe failures. This could require a blood patch and poses a risk of serious injury during medical procedures.
The LOR syringes in the kits can fail, leading to dural puncture. This may cause a leak of cerebrospinal fluid and require a blood patch to seal the hole. The risk is higher during spinal epidural procedures where precise needle placement is critical.
Healthcare professionals using the FlexTip Plus kits for spinal epidural procedures are most at risk. Patients receiving these procedures may also be affected if the kit is used incorrectly.
Check for product code ASK-05560-WH on the kit. Affected lots include 13F18L0892 through 13F19L0079. The kits are sold for medical use in hospitals and clinics.
Look for the lot numbers 13F18L0892 through 13F19L0079 on the FlexTip Plus kit packaging.
Yes, the LOR syringes can fail, causing dural puncture which may require a blood patch and pose a risk of serious injury during spinal epidural procedures.
Check the lot number on the kit. If it matches the affected lots (13F18L0892 through 13F19L0079), contact Arrow for guidance.
The recall record does not specify a replacement process. Contact Arrow directly for assistance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1184-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1184-2020 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.
