Home / Recalls / Medical Devices
Abbott Laboratories recalls ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott ARCHITECT cSystem is intended for In Vitro dia
Recalled July 29, 2015 · FDA recall Z-2202-2015 · Abbott Laboratories
Hazard
The ARCHITECT c8000 instrument contains tubing that does not meet specifications and has the potential to leak. · FDA Class II
Units
5 units
Sold at
US Nationwide Distribution in the states of CA, AL, NY and WI.
Description
The ARCHITECT c8000 instrument contains tubing that does not meet specifications and has the potential to leak.
Product
ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott ARCHITECT cSystem is intended for In Vitro diagnostic use only. It is designed to perform automated: chemistry tests, utilizing photometry and potentiometric technology.
Manufacturer(s)
Abbott Laboratories
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →