Burlington Medical recalls Blockers with Xenolite 800 attenuation material manufactured between January 2025 and January 2026 due to potential lifespan reduction from material degradation.
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical is recalling several Blockers models made with Xenolite 800 attenuation material from January 2025 to January 2026 because the material may degrade over time, reducing the device's lifespan. This recall affects users who own these specific models and could lead to shorter-than-expected device life.
The Xenolite 800 attenuation material used in these Blockers may degrade over time, causing the device to have a reduced lifespan. This means the product might not function as intended for as long as expected, but it does not pose an immediate safety hazard.
Users of the recalled Blockers models are most at risk if they own any of the 10 specific models listed in the recall. The risk is primarily for owners who use the devices long-term.
Check if your Blockers model has a serial number manufactured between January 16, 2025, and January 21, 2026. The affected models include R8BLOCKER1 through U8BLOCKER1 with specific UDI-DI (Product Codes) listed in the recall.
Identify your Blockers model number and compare it to the list of affected models provided in the recall.
No, only specific models made with Xenolite 800 attenuation material between January 16, 2025, and January 21, 2026 are affected.
The recall does not include a remedy, so no action is required beyond checking if your model is affected.
Check the model number and UDI-DI (Product Code) against the list of 10 specific models and dates provided in the recall.
We’ve drafted a message you can send Burlington Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1764-2026 — Burlington Medical Burlington Medical Hello, I own a Burlington Medical that is covered by recall Z-1764-2026 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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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.
