Carroll-Baccari, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0368-2020)

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:

Lemon Prep: MD0019T - 4 oz tubes MD0019--SUP - Single Use Cups Skin preparation used to enhance signal quality of patient recording electrodes (i.e. EKG, ECG, etc.)

Product Classification:

Class II

Date Initiated: September 5, 2019

Date Posted: November 20, 2019

Recall Number: Z-0368-2020

Event ID: 83827

Reason for Recall:

Product has the potential to be contaminated with Burholderia cepacia.

Status: Terminated

Product Quantity: 24,979 units

Code Information:

MD0019-T: 29824, 29901, 30006, 30145, 30236, 30352, 30675, 30729, 31138 MD0019-SUP: 29927, 30009, 30031, 30115, 30059, 30237, 30300, 30340, 30424, 30642, 30735, 31139

Distribution Pattern:

US, Canada, Spain, England, and Australia

Voluntary or Mandated:

Voluntary: Firm initiated