Ge Medical Systems Information Technologies
Tampa, FL
This page shows every FDA and USDA recall linked to Ge Medical Systems Information Technologies. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
8
Total Recalls
2000
First Recall
2004
Most Recent
Dinalink brand Communication Cable which is an accessory to a medical device Dinalike which is an isolated pro...
Jul 20, 2004
· Device
Terminated
Infant reusable blood pressure cuffs, one tube, male slip luer connector, P/N 2930 , manufactured for Welch Al...
Oct 15, 2003
· Device
Terminated
Critikon brand Omni-Sat Adult, Semi-Disposable Sensor - P/N 009136
Oct 15, 2003
· Device
Terminated
Critikon brand Omni-Stat Finger Sensor - P/N 009084
Oct 15, 2003
· Device
Terminated
Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors...
Oct 15, 2003
· Device
Terminated
Critikon brand Omni-Sat Neonatal, Semi-Disposable Sensor, P/N 009130
Oct 15, 2003
· Device
Terminated
GE Medical Systems COROMETRICS Maternal/Fetal Monitoring Systems, Models 2126is, 2128is, 2129is
Sep 23, 2003
· Device
Terminated
Critikon brand Adult, DURA-CUF, product code 2790, used as an arm cuff in association with a blood pressure mo...
Sep 17, 2003
· Device
Terminated