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Bard Peripheral Vascular Inc Recall 89553

Description: ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G

Bard Peripheral Vascular Inc Recall 89553 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0793-2022
Event ID89553
Event DescriptionADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G
Product TypeDevices
DistributionU.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.
Quantity1260 devices
Recall ReasonDue to lumbar puncture tray manometer failure mode of leaking and mating issues.
Device Classification20220323
Device Code InfoCatalog Number: 4301CDF Lot Numbers/UDI (GTIN, DI + PI): 0001433537 (01)10885403231810(17)260831(10)0001433537 0001437269 (01)10885403231810(17)260930(10)0001437269
Center Classification Date20220316
Recall Initiation Date20220120
Recalling FirmBard Peripheral Vascular Inc
Initial Notification Letter
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