The Recall Desk
HighFDA (Devices)·Z-1759-2026·Announced 2026-04-08

Burlington Medical protective sleeves may lose radiation attenuation over time

Burlington Medical is recalling protective sleeves made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Rubric level 3 covers risk-of-harm products where injury has not yet been reported: degraded attenuation reduces the radiation protection the product is worn to provide, and no injuries are stated.

Plain-English summary

Burlington Medical is recalling its protective sleeves, models R8SL and R8SL3. About 1,129 units were distributed nationwide in the United States and internationally to Canada, Australia, Bangladesh, Chile, Hong Kong, India, Mexico, Malaysia, Panama, Singapore, Thailand, Taiwan, Uruguay and Vietnam. The FDA has classified this recall as Class II.

There is potential for attenuation degradation over time, decreasing the lifespan of the product.

All serial numbers manufactured with Xenolite 800 attenuation material between 16 January 2025 and 21 January 2026 are affected, across UDI-DIs including 00840331271904 and 00840331271911.

Facilities can identify affected sleeves by the model number and UDI above, and may contact Burlington Medical for further information.

The recalled product

Product
Burlington Medical, Protective Sleeves.
Manufacturer
Burlington Medical, LLC
Category
Medical Device — Radiation protection
Hazard
Affected units
1,129

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (18)

  • UDI-DI (Product Code): 00840331271904 (SL8-R8SL). 2. Model Number: R8SL3
  • UDI-DI (Product Code): 00840331271911 (SL38-R8SL3-LG)
  • 00840331271928 (SL38-R8SL3-MD)
  • 00840331271935 (SL38-R8SL3-SM)
  • 00840186699816 (SL38-R8SL3-XL)
  • 00840331271942 (SL38-R8SL3-XS). 3. Model Number: S8SL
  • UDI-DI (Product Code): 00840331271959 (SL8-S8SL). 4. Model Number: S8SL3
  • UDI-DI (Product Code): 00840331271966 (SL38-S8SL3-LG)
  • 00840331271973 (SL38-S8SL3-MD)
  • 00840331271980 (SL38-S8SL3-SM)
  • 00840186699823 (SL38-S8SL3-XL)
  • 00840331271997 (SL38-S8SL3-XS). 5. Model Number: U8SL
  • UDI-DI (Product Code): 00840331272000 (SL8-U8SL). 6. Model Number: U8SL3
  • UDI-DI (Product Code): 00840331272017 (SL38-U8SL3-LG)
  • 00840331272024 (SL38-U8SL3-MD)
  • 00840331272031 (SL38-U8SL3-SM)
  • 00840186699830 (SL38-U8SL3-XL)
  • 00840331272048 (SL38-U8SL3-XS).

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 13 recalled by Burlington Medical, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 13 products in this recall →

Related recalls

Same manufacturer · Burlington Medical, LLC

See all →

Same hazard · attenuation degradation

See all →