Reported Apr 8, 2026 · Ongoing

Burlington Medical, Demi Half Aprons.

Burlington Medical, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Burlington Medical, LLC · 3 Elmhurst St · Newport News, VA · 23603-1137

Is this the product you have?

  • Burlington Medical, Demi Half Aprons.
Lot codes and dates
  • All serial numbers are affected that were manufactured with Xenolite 800 attenuation material from 01/16/2025 to 01/21/2026. 1
  • Model NumberR8DHALFR
  • UDI-DI (Product Code)
    • 00197513001485 (DHALF8-R8DHALFR-L)
    • 00197513001478 (DHALF8-R8DHALFR-M)
    • 00197513001461 (DHALF8-R8DHALFR-S)
    • 00197513001492 (DHALF8-R8DHALFR-XL)
    • 00197513001607 (DHALFSET8-R8DHALFR-SET)
Amount recalled
29 units

This recall covers 13 products

The agency filed one notice per product. You are reading one of them; the other 12 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for attenuation degradation over time, decreasing the lifespan.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.