Arrow International Inc recalls Epidural Catheterization Kit with FlexTip Plus, Open Tip, Si
Recalled Product
Epidural Catheterization Kit with FlexTip Plus, Open Tip, Single- Port Catheter, Product Code ASK-05502-NY
Hazard / Issue
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.
Issued by
FDA
Affected States: AK, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WY
Lot/Code Info: Lots: 23F19C0385 23F19G0310 23F19H0234 23F19K0248 23F19F0167 23F19G0434 23F19J0063
View official government recall
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