FDA recall Z-0717-2021

B Braun Medical, Inc. · Class II · device

Product

APEX Compounding System Control Panel Module, REF: 601224, Product Code AX1000 - Product Usage: intended for intravascular administration to a patient.

Reason for recall

There is the potential for the compounding system to not immediately interrupt compounding and alert user to the presence of an air bubble exceeding 3% of the ordered volume for an ingredient. This could result in a a compounded drug that does not meet the specified accuracy range for an individual ingredient.

Distribution

US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, IL, LA, MA, MD, MI, MN, MO, NC, NH, NJ, NV, NY, OH, OK, PA, TN,TX, WA.

Key facts

Status
Terminated
Initiation date
2020-11-23
Report date
2020-12-30
Termination date
2023-03-14
Voluntary/Mandated
Voluntary: Firm initiated
Location
Carrollton, TX, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0717-2021