FDA Recall
Terminated
Power cord for Model 3300 Cardiac Output Computer, List # 41245-04-03, AC cord manufactured by Electri-Cord, Westfield PA, Infusion pumps manufactured by Hospira, Morgan Hill, CA.
Recall: Z-0142-2010
·
Initiated August 11, 2009
Recall
- Recall Number
- Z-0142-2010
- Event Number
- 53257
- Firm
- Hospira Inc
- FEI Number
- 2921482
- Product Code
- dxg
- Status
- Terminated
- Root Cause
- Component design/selection
- Initiated
- August 11, 2009
- Posted
- November 9, 2009
- Terminated
- April 4, 2012
Description
Power cord for Model 3300 Cardiac Output Computer, List # 41245-04-03, AC cord manufactured by Electri-Cord, Westfield PA, Infusion pumps manufactured by Hospira, Morgan Hill, CA.
Reason
Fire/Shock hazard-- The power cord used in the device may cause sparks/flashes and poses a fire and shock hazard.
Action
Hospira initiated its recall on 08/14/2009. A nationwide press release was issued to AP, and a letter to consignees was sent via UPS. The firm will replace affected cords and effectiveness checks will be conducted through tracking of servicing.
Distribution
Worldwide distribution.
Quantity
204,999 power cords distributed for all devices