Bard Lumbar Puncture Tray Recall: Manometer Leaks Risk Injury

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Contact the company & request your remedy

Recalling firmBard Peripheral Vascular Inc1625 W 3rd St Bldg 1, N/A · Tempe, AZ 85281-2438

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Bard is recalling adult lumbar puncture trays that may leak due to manometer failure. This could lead to injury during medical procedures if the tray is used improperly.

Why it’s dangerous

The manometer in the tray can leak, causing improper pressure readings during spinal procedures. This might lead to injury if the tray is used without proper monitoring.

Who’s affected

Healthcare professionals using the recalled lumbar puncture trays are most at risk. Patients receiving procedures with these trays may also be affected.

How to tell if you have this one

Check for catalog number 4306CW. Lot numbers include 0001415028, 0001417842, 0001424355, 0001431413, and 0001436376 with specific dates.

Brand
Bard
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Tray Catalog Number
Look for catalog number 4306CW on the tray's label.
Contact Manufacturer
Reach out to Bard Peripheral Vascular Inc for further assistance if you have the recalled tray.

✎ GovInfoNow

Questions people ask

Why is this tray being recalled?

The manometer in the tray can leak, causing improper pressure readings during spinal procedures which might lead to injury.

What should I do if I have this tray?

Check the catalog number and lot numbers listed in the recall notice. Contact Bard Peripheral Vascular Inc for further instructions.

Is there a risk of serious injury?

The recall states that manometer leaks could lead to injury during medical procedures, but the exact risk level is not specified in the notice.

Take action

Contact Bard

We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0798-2022 — Bard Bard

Hello,

I own a Bard that is covered by recall Z-0798-2022 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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Where this comes from

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.

Official source: FDA Recall #Z-0798-2022 (January 20, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0798-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Bard Peripheral Vascular Inc recalls ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY

Use caution until it’s fixed