Carroll-Baccari, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1551-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Wave Prep Tubes (1710-03) and single use cups (17--00-24)

Product Classification:

Class II

Date Initiated: December 23, 2019

Date Posted: April 1, 2020

Recall Number: Z-1551-2020

Event ID: 84587

Reason for Recall:

Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug Administration inspection on October 15, 2019 were tested and found to be contaminated with Burkholderia cepacia. Mavidon is recalling all products manufactured at their facility.

Status: Terminated

Product Quantity: 1444 units

Code Information:

All Lots

Distribution Pattern:

Nationwide, Canada, UK, Spain, Australia

Voluntary or Mandated:

Voluntary: Firm initiated