Burlington Medical recalls certain Caps models manufactured between January 2025 and January 2026 due to potential attenuation material degradation over time, reducing lifespan.
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical is recalling specific Caps models made from January 2025 to January 2026 because the internal material may degrade over time, shortening their lifespan. This does not pose an immediate safety risk but could lead to premature failure.
The Caps contain Xenolite 800 attenuation material that may degrade over time, causing the product to have a shorter lifespan than expected. This degradation does not cause immediate harm but could lead to premature failure of the device.
Users of the recalled Caps models, particularly those with the specific model numbers R8CAP, S8CAP, or U8CAP manufactured between January 2025 and January 2026, are affected. The risk is minimal as the issue relates to reduced lifespan rather than safety hazards.
Check for model numbers R8CAP, S8CAP, or U8CAP with serial numbers manufactured between January 2025 and January 2026. The product codes include specific combinations like CAP8-R8CAP-LG_XL or CAP8-U8CAP-SM_MD.
Identify if your Caps model is R8CAP, S8CAP, or U8CAP with serial numbers manufactured between January 2025 and January 2026.
The affected models are R8CAP, S8CAP, and U8CAP with specific product codes and serial numbers manufactured between January 2025 and January 2026.
No, the recall is for potential lifespan reduction, not an immediate safety hazard. The product does not pose a risk of injury.
Check the model number and serial date range: R8CAP, S8CAP, or U8CAP manufactured between January 2025 and January 2026 with specific product codes.
We’ve drafted a message you can send Burlington Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1760-2026 — Burlington Medical Burlington Medical Hello, I own a Burlington Medical that is covered by recall Z-1760-2026 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.
