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Bard Peripheral Vascular Inc recalls LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
Recalled March 23, 2022 · FDA recall Z-0795-2022 · Bard Peripheral Vascular
Hazard
Due to lumbar puncture tray manometer failure mode of leaking and mating issues. · FDA Class II
Units
8,630 devices
Sold at
U.S. Nationwide Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, Puerto Rico, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. O.U.S. (foreign) including states: Costa Rica and Hong Kong.
Description
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Product
LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
Manufacturer(s)
Bard Peripheral Vascular Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →