Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LEO

Recalled February 19, 2020 · FDA recall Z-1186-2020 · Arrow International

Hazard

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. · FDA Class II

Units

343,105 total

Sold at

The products were distributed to the following US 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, and WY.

Description

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.

Product

EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LEO

Manufacturer(s)

Arrow International Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →