RecallRadar

FDA Device recall Z-0795-2022

LUMBAR PUNCTURE TRAY ADULT 18G X 3.5

On 2022-03-23 the FDA classified a Class II recall of LUMBAR PUNCTURE TRAY ADULT 18G X 3.5 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-0795-2022
ClassificationClass II
Statusongoing
Initiated2022-01-20
Published2022-03-23
Last updated2026-09-13 11:56 UTC
CompanyBard Peripheral Vascular
DistributionUS

Product

LUMBAR PUNCTURE TRAY ADULT 18G X 3.5

Reason

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

Identifiers

code_info
Catalog Number: 4303C Lot Numbers/UDI (GTIN, DI + PI): 0001411294 (01)10885403057021(17)220331(10)0001411294 0001414259…Catalog Number: 4303C Lot Numbers/UDI (GTIN, DI + PI): 0001411294 (01)10885403057021(17)220331(10)0001411294 0001414259 (01)10885403057021(17)220331(10)0001414259 0001414361 (01)10885403057021(17)220331(10)0001414361 0001415025 (01)10885403057021(17)220430(10)0001415025 0001417547 (01)10885403057021(17)220430(10)0001417547 0001422377 (01)10885403057021(17)220630(10)0001422377 0001425366 (01)10885403057021(17)220630(10)0001425366 0001426588 (01)10885403057021(17)220630(10)0001426588 0001428500 (01)10885403057021(17)220630(10)0001428500 0001431408 (01)10885403057021(17)220630(10)0001431408 0001433267 (01)10885403057021(17)220831(10)0001433267 0001433868 (01)10885403057021(17)220930(10)0001433868

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-0795-2022%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.