FDA Device recall Z-0799-2022
LUMBAR PUNCTURE DRUG FREE TRAY 22G
- FDA Device
- Class II
- ongoing
- Published 2022-03-23
On 2022-03-23 the FDA classified a Class II recall of LUMBAR PUNCTURE DRUG FREE TRAY 22G 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-0799-2022 |
| 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 DRUG FREE TRAY 22G
Reason
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Identifiers
| code_info | Catalog Number: 4306CWDF Lot Numbers/UDI (GTIN, DI + PI): 0001415023 (01)10885403231827(17)250731(10)0001415023 0001416…Catalog Number: 4306CWDF Lot Numbers/UDI (GTIN, DI + PI): 0001415023 (01)10885403231827(17)250731(10)0001415023 0001416353 (01)10885403231827(17)250731(10)0001416353 0001420159 (01)10885403231827(17)250731(10)0001420159 0001424771 (01)10885403231827(17)250731(10)0001424771 0001437270 (01)10885403231827(17)250731(10)0001437270 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
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All Bard Peripheral Vascular recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0799-2022%22
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