Burlington Medical, LLC: Medical Device Recall in 2019 - (Recall #: Z-2125-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Front/Back Apron with Stretch Velcro Closure, Product Number EURO, Part Numbers ECSEEUROA, ECSEEUROB, ECSEEUROC, ECSEEUROXLM, REEURO*F, REEURO*M, REEUROC, REEUROE, SEEURO*F, SEEURO*M, UEEURO*F Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount of radiation reaching the user.

Product Classification:

Class II

Date Initiated: June 7, 2019

Date Posted: August 7, 2019

Recall Number: Z-2125-2019

Event ID: 83144

Reason for Recall:

The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter radiation of varying degrees depending on many different variables (e.g., distance, shielding, position, time, kV, etc.). Long-term exposure to scatter radiation may increase the risk of cancer, infertility, or other health-related conditions.

Status: Terminated

Product Quantity: 48

Code Information:

Serial Numbers: 381839 382008 381834 423928 423922 423917 423919 423921 423916 387073 423925 387072 423918 419789 387168 423923 423926 423924 387116 391152 381819 381824 391111 391093 387078 381786 382901 419907 419906 403296 382883 387075 391159 382894 391166 418938 387975 418911 382881 403349 405569 443366 377104 423704 403406 419550 419902 419903

Distribution Pattern:

US Nationwide distribution. The products were distributed to the following foreign countries: Korea, Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated