GE Medical Systems Information Technologies GE Medical Systems COROMETRICS Maternal/Fetal Monitoring Systems, Models 2126is, 2128is, 2129is Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
GE Medical Systems COROMETRICS Maternal/Fetal Monitoring Systems, Models 2126is, 2128is, 2129is
Brand
GE Medical Systems Information Technologies
Lot Codes / Batch Numbers
All serial numbers are involved.
Products Sold
All serial numbers are involved.
GE Medical Systems Information Technologies is recalling GE Medical Systems COROMETRICS Maternal/Fetal Monitoring Systems, Models 2126is, 2128is, 2129is due to The 2120 Main Board on device lacks required external safety 'watchdog' circuit.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The 2120 Main Board on device lacks required external safety 'watchdog' circuit.
Recommended Action
Per FDA guidance
The firm mailed or faxed a recall letter to consignees on May 14, 2003 followed by a phone call to each account within two weeks to arrange for a service technician visit to correct the monitors. The recall letter warned the hospitals of the problem and a work around.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, IN, MD, MN, NV, SC, TX, WI
Page updated: Jan 10, 2026