FDA Device recall Z-0791-2022
LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
- FDA Device
- Class II
- ongoing
- Published 2022-03-23
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
| Agency | FDA Device |
|---|---|
| Recall number | Z-0791-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-01-20 |
| Published | 2022-03-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Bard Peripheral Vascular |
| Distribution | US |
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
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