B1DMVP — GovInfoNow

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Contact the company & request your remedy

Recalling firmPhilips Ultrasound, Inc1 Echo Dr · Reedsville, PA 17084-8603

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

B1DMVP

Why it’s dangerous

This product is a medical device that is used for ultrasound imaging. The product name B1DMVP is a specific model of ultrasound device from Philips Ultrasound, Inc. The product is designed for medical use and is not intended for consumer use. The product is not dangerous to the general public as it is a medical device that is used under the supervision of healthcare professionals. However, if the device is misused or if there are issues with the device's performance, it could pose a risk to patients. The product is not a consumer product and is not intended for sale to the general public.

Who’s affected

All

How to tell if you have this one

Check the product's specifications and ensure it is used by qualified healthcare professionals. Ensure the device is properly maintained and calibrated. Check for any recalls or warnings from the manufacturer.

Brand
B1DMVP
Category
Medical device

Based on the official FDA remedy

What to do — step by step

1
Verify that the product is being used by qualified healthcare professionals.
2
Ensure the device is properly maintained and calibrated according to the manufacturer's guidelines.
3
Check for any recalls or warnings from the manufacturer or regulatory bodies.

✎ GovInfoNow

Questions people ask

Is this product safe for general use?

No, this product is a medical device and is not intended for general consumer use. It is designed for use by healthcare professionals in medical settings.

What are the risks of using this product incorrectly?

If the device is misused or if there are issues with the device's performance, it could pose a risk to patients. For example, incorrect use could lead to inaccurate imaging results, which could affect diagnosis and treatment.

How often should this device be maintained and calibrated?

The device should be maintained and calibrated according to the manufacturer's guidelines, which typically include regular checks and periodic calibrations to ensure accuracy and safety.

Take action

Contact B1DMVP

We’ve drafted a message you can send B1DMVP to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2066-2025 — B1DMVP B1DMVP

Hello,

I own a B1DMVP that is covered by recall Z-2066-2025 from B1DMVP.

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-2066-2025 (May 28, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2066-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.

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