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Bard Peripheral Vascular Inc recalls LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL
Recalled March 23, 2022 · FDA recall Z-0796-2022 · Bard Peripheral Vascular
Hazard
Due to lumbar puncture tray manometer failure mode of leaking and mating issues. · FDA Class II
Units
29,870 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 22G X3.5 STRL
Manufacturer(s)
Bard Peripheral Vascular Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →