Verathon BladderScan Prime Plus Probe Handle May Crack - Recall

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Recalling firmVerathon, Inc.20001 N Creek Pkwy, N/A · Bothell, WA 98011-8218

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Verathon is recalling BladderScan Prime Plus Probes with serial numbers starting with P1500000 due to a potential handle crack. This could cause the probe to break during use, leading to injury or damage.

Why it’s dangerous

The probe handle may crack due to a change in material and manufacturing process. If the handle cracks, the probe could break during use, potentially causing injury or damage to the user.

Who’s affected

Users of the BladderScan Prime Plus Probe for measuring urine volume are affected. Those with the specific serial numbers listed in the recall are most at risk.

How to tell if you have this one

Check if your BladderScan Prime Plus Probe has a serial number starting with P1500000. The specific serial numbers are listed in the recall notice.

Brand
Verathon
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Handle Condition
Inspect the probe handle for cracks or signs of damage before use.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The probe handle may crack due to a change in material and manufacturing process.

What should I do if I have this product?

Check the handle for cracks. If it cracks, stop using the probe immediately.

How can I tell if my product is affected?

Your product is affected if it has a serial number starting with P1500000, as listed in the recall notice.

Take action

Contact Verathon

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

✉️ Open in email

Subject: Recall Z-0531-2021 — Verathon Verathon

Hello,

I own a Verathon that is covered by recall Z-0531-2021 from Verathon.

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-0531-2021 (September 29, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0531-2021 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.

Verathon, Inc. recalls BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the

Lower-risk recall