Malvern Panalytical NanoSight NS300 Laser Safety Recall

Take action

Contact the company & request your remedy

Recalling firmMALVERN PANALYTICAL LTDGrovewood Road, N/A · Malvern, N/A N/A

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Malvern Panalytical is recalling its NanoSight NS300 devices because they do not meet Class 1 laser safety requirements. This could lead to potential risks if the device is used without proper safety measures.

Why it’s dangerous

The device fails to meet Class 1 laser safety standards, which are designed to ensure minimal risk of harm from laser radiation. If the device is used without proper safety protocols, there could be potential exposure to laser radiation.

Who’s affected

Users of the NanoSight NS300 device are affected. Laboratory personnel and researchers using the device are most at risk due to potential laser exposure.

How to tell if you have this one

The NanoSight NS300 device with CDRH accession #0510530-003 is affected. This product was sold by Malvern Panalytical.

Brand
Malvern Panalytical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Status
Verify if your NanoSight NS300 has the CDRH accession number 0510530-003.

✎ GovInfoNow

Questions people ask

Is this device dangerous?

The device does not meet Class 1 laser safety requirements, which could pose risks if used improperly.

What should I do if I have this device?

Check if your device has the CDRH accession number 0510530-003. If so, contact Malvern Panalytical for further instructions.

How can I be sure my device is affected?

The affected device has the CDRH accession number 0510530-003, which is listed in the recall notice.

Take action

Contact Malvern Panalytical

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

✉️ Open in email

Subject: Recall Z-1442-2022 — Malvern Panalytical Malvern Panalytical

Hello,

I own a Malvern Panalytical that is covered by recall Z-1442-2022 from Malvern Panalytical.

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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-1442-2022 (April 7, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1442-2022 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.

MALVERN PANALYTICAL LTD recalls NanoSight NS300

Lower-risk recall