Z-0142-2010

Power cord for Model 3300 Cardiac Output Computer, List # 41245-04-03, AC cord manufactured by Electri-Cord...

Name: Z-0142-2010 Power cord for Model 3300 Cardiac Output Computer, List # 41245-04-03, AC cord manufactured by Electri-Cord...
Creator: Hospira Inc
Published: 2009-08-11
License: https://open.fda.gov/license/

Abbott Medical / initiated 2009-08-11 / Terminated / root cause: design

FDA source

Hospira Inc began a recall of Power cord for Model 3300 Cardiac Output Computer, List # 41245-04-03, AC cord manufactured by Electri-Cord, Westfield PA, Infusion pumps manufactured by... on 2009-08-11. The reason FDA records is "Fire/Shock hazard-- The power cord used in the device may cause sparks/flashes and poses a fire and shock hazard". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-0142-2010
Status: Terminated
Initiated: 2009-08-11
Posted: 2009-11-09
Terminated: 2012-04-04
Recalling firm: Abbott Medical
Product: 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.
Product code: dxg
Reason for recall: Fire/Shock hazard-- The power cord used in the device may cause sparks/flashes and poses a fire and shock hazard.
Root cause tag: design
FDA root cause: Component design/selection
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.
Quantity in commerce: 204,999 power cords distributed for all devices
Distribution: Worldwide distribution.
Product codes and lots: AC power cords, all units of Part Numbers: 826-85559-001, 826-85559-003, 826-85559-008, 826-85559-010, 826-96057-003

Product code dxg

K932414Class IIContinuous Cardiac Output SystemAbbott Laboratories / cleared 1994-11-14

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)