Arrow International Inc recalls FlexTip Plus Epidural Catheterization Kit, Product Code ASK-
Recalled Product
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH
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: 23F19A0240 23F19G0305 23F19J0292 23F19L0414 23F19E0112 23F19G0496 23F19K0152
View official government recall
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