Bard Peripheral Vascular Inc recalls ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY

Recalled March 23, 2022 · FDA recall Z-0798-2022 · Bard Peripheral Vascular

Hazard

Due to lumbar puncture tray manometer failure mode of leaking and mating issues. · FDA Class II

Units

2,880 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

ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY

Manufacturer(s)

Bard Peripheral Vascular Inc

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