FDA Device recall Z-0792-2022

LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP

• FDA Device
• Class II
• ongoing
• Published 2022-03-23

On 2022-03-23 the FDA classified a Class II recall of LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP by Bard Peripheral Vascular, citing due to lumbar puncture tray manometer failure mode of leaking and mating issues.

Read the official FDA Device notice

Product

LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP

Reason

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

Identifiers

Status history

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

Other recalls by Bard Peripheral Vascular

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• Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
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• Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T
  FDA Device · Class II · 2025-12-17 · Bard Peripheral Vascular
• Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the Venclose EVSRF Ablation…
  FDA Device · Class II · 2025-10-08 · Bard Peripheral Vascular
• Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236
  FDA Device · Class I · 2025-03-12 · Bard Peripheral Vascular

All Bard Peripheral Vascular recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0792-2022%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.