Arrow International Inc recalls FlexTip Plus Epidural Catheterization Set, Product Code AA-0
Recalled Product
FlexTip Plus Epidural Catheterization Set, Product Code AA-05400-E
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: 71F19B2081 71F19C1655 71F19E2128 71F19G2444 71F19B2586 71F19E1245 71F19F1432 71F19J1685
View official government recall
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