The Recall Desk
HighFDA (Devices)·Z-1757-2026·Announced 2026-04-08

[pending] Burlington Medical, Wrap Aprons.

Pending LLM rewrite. Source: FDA_DEVICE Z-1757-2026.

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: Pending LLM scoring against the rubric.

Plain-English summary

Potential for attenuation degradation over time, decreasing the lifespan.

The recalled product

Product
Burlington Medical, Wrap Aprons.
Manufacturer
Burlington Medical, LLC
Category
Medical Device — Devices

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 (20)

  • UDI-DI (Product Code): 00840331297683 (WRAPC8-C8EURO-LF )
  • 00840331297683 (WRAPC8-C8EURO-LM )
  • 00840331297683 (WRAPC8-C8EURO-MF )
  • 00840331297683 (WRAPC8-C8EURO-MM )
  • 00840331297683 (WRAPC8-C8EURO-SF )
  • 00840331297683 (WRAPC8-C8EURO-SM )
  • 00840331297683 (WRAPC8-C8EURO-XLM )
  • 00840331297683 (WRAPT18-C8EURO-LF )
  • 00840331297683 (WRAPT18-C8EURO-LM )
  • 00840331297683 (WRAPT18-C8EURO-MM )
  • 00840331297683 (WRAPT18-C8EURO-PLUS )
  • 00840331297683 (WRAPT18-C8EURO-SM ). 2. Model Number: C8F111
  • UDI-DI (Product Code): 00840331258721 (WRAPC18-R8EURO-2XF )
  • 00840331258738 (WRAPC18-R8EURO-2XM )
  • 00840331258745 (WRAPC18-R8EURO-3XF )
  • 00840331258752 (WRAPC18-R8EURO-3XM )
  • 00840331258769 (WRAPC8-R8EURO-LF )
  • 00840331258776 (WRAPC8-R8EURO-LM )
  • 00840331258783 (WRAPC8-R8EURO-MF )
  • 00840331258790 (WRAPC8-R8EURO-MM )

Distribution

Distributed nationwide across the United States.

Related recalls

Same category