Recall of Burlington Medical Half Aprons for Attenuation Degradation
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Burlington Medical, LLC is recalling 402 units of its half aprons due to potential attenuation degradation over time, which could decrease their lifespan and effectiveness.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 15, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
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Recall of Burlington Medical Half Aprons
What Happened
Burlington Medical, LLC is initiating a voluntary recall of certain half aprons due to a potential for attenuation degradation over time, which may decrease the product's lifespan and protective capabilities.
Which Products Are Affected
The recall involves 402 units of Burlington Medical Half Aprons manufactured with Xenolite 800 attenuation material from January 16, 2025, to January 21, 2026. Affected models include: 1. Model Number: R8HALF1B; UDI-DI: 00840331272291. 2. Model Number: R8HALF1H; UDI-DI: 00840331272314. 3. Model Number: R8HALF2B; UDI-DI: 00840331272338. 4. Model Number: R8HALF2H; UDI-DI: 00840331272345. 5. Model Number: R8HALF3B; UDI-DI: 00840331272352. 6. Model Number: R8HALF3H; UDI-DI: 00840331272369. 7. Model Number: R8HALF4B; UDI-DI: 00840331272376. 8. Model Number: R8HALF4H; UDI-DI: 00840331272383. 9. Model Number: R8HALF5B; UDI-DI: 00840331272390. 10. Model Number: R8HALF5H; UDI-DI: 00840331272406. 11. Model Number: R8HALF6B; UDI-DI: 00840331272420. 12. Model Number: R8HALF6H; UDI-DI: 00840331272352. 13. Model Number: R8HALFSETB; UDI-DI: 00840331272413. 14. Model Number: R8HALFSETH; UDI-DI: 00840331272420. 15. Model Number: S8HALF1H; UDI-DI: 00840331272451. 16. Model Number: S8HALF2B; UDI-DI: 00840331272475. 17. Model Number: S8HALF2H; UDI-DI: 00840331272482. 18. Model Number: S8HALF3B; UDI-DI: 00840331272499. 19. Model Number: S8HALF3H; UDI-DI: 00840331272505. 20. Model Number: S8HALF4B; UDI-DI: 00840331272512. 21. Model Number: S8HALF4H; UDI-DI: 00840331272529. 22. Model Number: S8HALF5B; UDI-DI: 00840331272536. 23. Model Number: S8HALF5H; UDI-DI: 00840331272543. 24. Model Number: S8HALF6H; UDI-DI: 00840331272499. 25. Model Number: S8HALFSETH; UDI-DI: 00840331272567. 26. Model Number: U8HALF3B; UDI-DI: 00840331272635. 27. Model Number: U8HALF3H; UDI-DI: 00840331272642. 28. Model Number: U8HALF4H; UDI-DI: 00840331272666. 29. Model Number: U8HALF5H; UDI-DI: 00840331272680. 30. Model Number: U8HALF6H; UDI-DI: 00840331272635. These products were distributed nationwide in the United States and internationally.
What You Should Do
Consumers who have these affected products should contact Burlington Medical, LLC for further instructions, as the recall was initiated via letter. The firm's address is 3 Elmhurst St, Suite 112, Newport News, VA 23603-1137.
Why This Matters
This recall affects 402 units of medical devices, potentially compromising their protective function and user safety due to degradation issues.
Source
This information is from the FDA recall database. For more details, visit the FDA website at https://www.fda.gov and search for recall number Z-1762-2026.
Original source: FDA Official Notice ↗
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