Bard recalls pediatric lumbar puncture trays with potential manometer leaks. Affected units have specific lot numbers; stop using immediately to prevent injury.
Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Bard is recalling pediatric lumbar puncture trays that may leak due to manometer failure. This could cause inaccurate pressure readings during medical procedures, potentially leading to complications for children.
The manometer in the tray can leak, causing inaccurate pressure readings during lumbar punctures. This may lead to complications like infection or bleeding in children.
Healthcare professionals using the recalled pediatric lumbar puncture trays for medical procedures. Children receiving lumbar punctures are at risk of complications if the tray leaks.
Check for the product name 'LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5' with specific lot numbers listed in the recall notice. The catalog number is 4304C.
Discontinue use of the recalled lumbar puncture tray to prevent inaccurate pressure readings during medical procedures.
The recalled model is LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 with catalog number 4304C.
Check for the product name 'LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5' and the specific lot numbers listed in the recall notice.
The recall does not mention a fix; the remedy is null, so users should stop using the product immediately.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0791-2022 — Bard Bard Hello, I own a Bard that is covered by recall Z-0791-2022 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.