Burlington Medical Kilt: Potential attenuation degradation over time

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Recalling firmBurlington Medical, LLC3 Elmhurst St, Suite 112 · Newport News, VA 23603-1137

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Burlington Medical is recalling Kilt devices made with Xenolite 800 attenuation material between January 2025 and January 2026. These devices may experience reduced lifespan over time due to material degradation.

Why it’s dangerous

The Xenolite 800 attenuation material used in these devices may degrade over time, leading to a reduced lifespan. This is a material durability issue that does not pose an immediate safety hazard.

Who’s affected

Users of Kilt devices with specific model numbers and serial numbers manufactured between January 2025 and January 2026. The risk is minimal as the issue affects lifespan rather than safety.

How to tell if you have this one

Check if your Kilt device has a model number (C8K303, R8K303, R8KILT, R8S302, R8SKIRT, S8K303, S8KILT, S8S302, S8SKIRT, U8K303, U8KILT, or U8S302) and was manufactured with Xenolite 800 attenuation material from January 2025 to January 2026.

Brand
Burlington Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Model
Identify your Kilt device's model number from the list provided in the recall notice.
Verify Manufacturing Date
Confirm your device was manufactured between January 2025 and January 2026 using the serial numbers or UDI-DI codes listed.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The recall is due to potential attenuation degradation over time in devices made with Xenolite 800 material, which may reduce the device's lifespan.

Do I need to stop using my Kilt device?

No, the recall does not require immediate discontinuation of use. The issue affects lifespan rather than safety.

How can I check if my device is affected?

Check your device's model number against the list of affected models and verify the manufacturing date was between January 2025 and January 2026.

Take action

Contact Burlington Medical

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

✉️ Open in email

Subject: Recall Z-1755-2026 — Burlington Medical Burlington Medical

Hello,

I own a Burlington Medical that is covered by recall Z-1755-2026 from Burlington Medical.

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-1755-2026 (February 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1755-2026 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.

Burlington Medical, LLC recalls Burlington Medical, Kilt

Lower-risk recall