GE Medical Systems Information Technologies Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug.
Brand
GE Medical Systems Information Technologies
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot numbers 01-08 through 02-16 which are embossed into the power cord metal blades and also those with no lot numbers.
GE Medical Systems Information Technologies is recalling Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient due to Reports of broken plug ground pins on AC power cords for patient monitors.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reports of broken plug ground pins on AC power cords for patient monitors.
Recommended Action
Per FDA guidance
The recalling firm mailed a Recall Notification Letter with response form and corretive power cords beginning on April 30, 2003 until August 14, 2003 as corrective cords became available. Consignees were instructed on how to determine if they have the recalled cords and to destroy any found by cutting the plug from the wire. Also corrective AC power cords were provided to each consignee.
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 noticePage updated: Jan 10, 2026