FDA Device recall Z-0794-2022

SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT

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

On 2022-03-23 the FDA classified a Class II recall of SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT 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

SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT

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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  FDA Device · Class II · 2026-10-07 · Bard Peripheral Vascular
• Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
  FDA Device · Class II · 2026-02-25 · Bard Peripheral Vascular
• 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-0794-2022%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.