Burlington Medical recalls Wrap Aprons with Xenolite 800 attenuation material manufactured from January 16, 2025 to January 21, 2026 due to potential degradation over time.
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical is recalling Wrap Aprons made with Xenolite 800 attenuation material between January 16, 2025 and January 21, 2026. These aprons may degrade over time, reducing their lifespan but not posing an immediate safety risk.
The Xenolite 800 attenuation material in these aprons may degrade over time, leading to a shorter lifespan. However, this does not cause immediate safety risks like injury or damage.
Users of Wrap Aprons with specific model numbers and serial numbers manufactured between January 16, 2025 and January 21, 2026 are affected. The risk is minimal as the issue relates to reduced lifespan rather than safety hazards.
Check for model numbers (e.g., C8EURO, R8EURO) and specific UDI-DI (Product Codes) listed in the recall notice. The aprons were manufactured between January 16, 2025 and January 21, 2026.
Review the model number and UDI-DI (Product Code) on your Wrap Apron to see if it matches the affected models listed in the recall.
No, the recall is for potential attenuation degradation over time, which reduces lifespan but does not cause safety risks like injury or damage.
The recall does not specify a remedy, so no action is required beyond checking if your apron is affected.
The affected aprons were manufactured between January 16, 2025 and January 21, 2026.
We’ve drafted a message you can send Burlington Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1757-2026 — Burlington Medical Burlington Medical Hello, I own a Burlington Medical that is covered by recall Z-1757-2026 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.
