Devices

ElectriCord

Model / Serial
Lot numbers 01-08 through 02-16 which are embossed into the power cord metal blades and also those with no lot numbers.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The recalled AC power cords were distributed to approximately 2600 Domestic hospital accounts nationwide and 180 international accounts.
Product Description
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.
Manufacturer
GE Medical Systems Information Technologies
1 Event
- Recall of ElectriCord

Manufacturer

GE Medical Systems Information Technologies

Manufacturer Address
GE Medical Systems Information Technologies, 4502 Woodland Corporate Blvd., Tampa FL 33614
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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