FDA Device recall Z-0796-2022

LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL

• 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 22G X3.5 STRL 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 22G X3.5 STRL

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.

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All Bard Peripheral Vascular recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0796-2022%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.