Burlington Medical recalls protective sleeves with Xenolite 800 material produced between Jan 2025 and Jan 2026 due to potential lifespan reduction from material degradation.
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical is recalling protective sleeves made with Xenolite 800 material from January 2025 to January 2026. These sleeves may degrade over time, reducing their lifespan and potentially causing them to fail earlier than expected.
The protective sleeves contain Xenolite 800 attenuation material that can degrade over time, leading to a reduced lifespan. This degradation may cause the sleeves to fail earlier than intended, but the hazard does not involve immediate risks like injury or fire.
Users of Burlington Medical protective sleeves with serial numbers manufactured between January 2025 and January 2026 are affected. Those using these sleeves for medical purposes may be at slightly higher risk due to potential premature failure.
Check for model numbers R8SL, R8SL3, S8SL, S8SL3, U8SL, or U8SL3 with specific product codes listed in the recall notice. These sleeves were manufactured from January 16, 2025, to January 21, 2026.
Identify your sleeve's model number and product code to confirm if it's in the recall list.
No, only sleeves manufactured with Xenolite 800 material from January 16, 2025, to January 21, 2026 are affected.
The recall does not specify a remedy, so contact Burlington Medical directly for guidance.
The recall does not provide information on how to identify degraded sleeves.
We’ve drafted a message you can send Burlington Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1759-2026 — Burlington Medical Burlington Medical Hello, I own a Burlington Medical that is covered by recall Z-1759-2026 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.
