RecallRadar

FDA Device recall Z-0791-2022

LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5

On 2022-03-23 the FDA classified a Class II recall of LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 by Bard Peripheral Vascular, citing due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0791-2022
ClassificationClass II
Statusongoing
Initiated2022-01-20
Published2022-03-23
Last updated2026-09-13 11:56 UTC
CompanyBard Peripheral Vascular
DistributionUS

Product

LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5

Reason

Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Identifiers

code_info
Catalog Number: 4304C Lot Numbers/UDI (GTIN, DI + PI): 0001414261 (01)10885403057052(17)220331(10)0001414261 0001414362…Catalog Number: 4304C Lot Numbers/UDI (GTIN, DI + PI): 0001414261 (01)10885403057052(17)220331(10)0001414261 0001414362 (01)10885403057052(17)220430(10)0001414362 0001415851 (01)10885403057052(17)220430(10)0001415851 0001415026 (01)10885403057052(17)220430(10)0001415026 0001421686 (01)10885403057052(17)220630(10)0001421686 0001424759 (01)10885403057052(17)220630(10)0001424759 0001426324 (01)10885403057052(17)220630(10)0001426324 0001428876 (01)10885403057052(17)220630(10)0001428876 0001432173 (01)10885403057052(17)220630(10)0001432173 0001434168 (01)10885403057052(17)220930(10)0001434168 0001438149 (01)10885403057052(17)221031(10)0001438149 0001438930 (01)10885403057052(17)221031(10)0001438930 0001441010 (01)10885403057052(17)221031(10)0001441010

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0791-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.