Burlington Medical, LLC recalls Burlington Medical
- Recalling company
- Burlington Medical, LLC
- Product
- Burlington Medical, Demi Half Aprons.
- Reason
- Potential for attenuation degradation over time, decreasing the lifespan.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 11, 2026
- Reported
- Apr 8, 2026
- Distribution
- Worldwide distribution. Nationwide distribution in the US and international distribution to Canada, Australia, Bangladesh, Chile, Hong Kong, India, Mexico, Malaysia, Panama, Singapore, Thailand, Taiwan, Uruguay, and Vietnam.
- Status
- Ongoing
- Quantity
- 29 units
- Lot / codes
- All serial numbers are affected that were manufactured with Xenolite 800 attenuation material from 01/16/2025 to 01/21/2026. 1. Model Number: R8DHALFR; UDI-DI (Product Code): 00197513001485 (DHALF8-R8DHALFR-L), 00197513001478 (DHALF8-R8DHALFR-M), 00197513001461 (DHALF8-R8DHALFR-S), 00197513001492 (DHALF8-R8DHALFR-XL), 00197513001607 (DHALFSET8-R8DHALFR-SET).
- Company location
- Newport News, VA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1763-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1763-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.