FDA recall Z-0368-2020

Carroll-Baccari, Inc. · Class II · device

Product

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.)

Reason for recall

Product has the potential to be contaminated with Burholderia cepacia.

Distribution

US, Canada, Spain, England, and Australia

Key facts

Status
Terminated
Initiation date
2019-09-05
Report date
2019-11-20
Termination date
2021-10-19
Voluntary/Mandated
Voluntary: Firm initiated
Location
Riviera Beach, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0368-2020