Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12
Recalled Product
EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12
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: 71F19A0623 71F19C1042 71F19E1144 71F19G2853 71F19K0248 71F19A2996 71F19C2596 71F19E2950 71F19H2549 71F19K2117 71F19B1149 71F19D2545 71F19G1138 71F19J1815 71F19L0436
View official government recall
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