Z-1596-2011

Hospira Power cord use on Symbiq One-Channel infuser and Symbiq Two-Channel infuser. Power cord part number...

Name: Z-1596-2011 Hospira Power cord use on Symbiq One-Channel infuser and Symbiq Two-Channel infuser. Power cord part number...
Creator: Hospira Inc
Published: 2010-10-27
License: https://open.fda.gov/license/

Abbott Medical / initiated 2010-10-27 / Terminated / root cause: design

FDA source

Hospira Inc began a recall of Hospira Power cord use on Symbiq One-Channel infuser and Symbiq Two-Channel infuser. Power cord part number: HSP3306-E07. Used on List No. 16026 - Symbiq One... on 2010-10-27. The reason FDA records is "Complaints of broken, bent or missing prongs, charring, sparks, visible smoke, burnt smell have been reported on Symbiq AC Power cords". 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-1596-2011
Status: Terminated
Initiated: 2010-10-27
Posted: 2011-03-08
Terminated: 2013-11-07
Recalling firm: Abbott Medical
Product: Hospira Power cord use on Symbiq One-Channel infuser and Symbiq Two-Channel infuser. Power cord part number: HSP3306-E07. Used on List No. 16026 - Symbiq One Channel infuser; List No. 16027 - Symbiq Two-Channel infuser
Product code: FRN Pump, Infusion
Reason for recall: Complaints of broken, bent or missing prongs, charring, sparks, visible smoke, burnt smell have been reported on Symbiq AC Power cords.
Root cause tag: design
FDA root cause: Component design/selection
Action: Hospira Recall notification letters were sent by Federal Express on November 1, 2010.
Quantity in commerce: 32,376 power cords
Distribution: Nationwide distribution and to Australia, Canada, and Malaysia.
Product codes and lots: Power cord part number: HSP3306-E07. Used on List No. 16026 - Symbiq One Channel infuser; List No. 16027 - Symbiq Two-Channel infuser List number configurations: 16026-04-01/03/04, 51/52,. 53/54, 79/80, 81/82, 83/84/ 87/88; 16027-04-01/03/04, 51/52, 53/54, 79/80, 81/82, 83/84, 87/88; 16026-13-25/26, 53/54; 16027-13-25/26, 53/54.

Product code FRN

K051550Class IIInspiration Ventilator SystemeVent Medical, Ltd. / cleared 2005-07-12

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)