Abbott Point Of Care Inc.: Medical Device Recalls in 2018
Updated on March 25, 2026.
According to to data from the FDA, there were 2 medical device recalls made by Abbott Point Of Care Inc. in 2018. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Abbott i-STAT CG8+ Cartridges intended for use in the in vitro quantification of potassium in arterial, venous, or capillary whole blood. List Number/UDI# : 03P88-25 ,(01)10054749000163(17)181028(10)L18059
- i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI: 00054749001255)