Atlas FDA

Hospira brand Plum A+I.V. Infusion Pump, List No. 11971-04; Hospira brand Plum A+I.V. Infusion Pump, List No. 12391-04;

FDA device recall Z-0389-06 · posted 2006-01-12 · Terminated

Recall details

Recalling firm
Hospira Inc
Reason for recall
The pump may shut-off prematurely during battery operation without providing adequate response time when 'E320' service warning message appears.
Action taken
On 5/18/05, the firm issued letters via Federal Express to all its direct consignees, informing them of the affected products and providing instructions on the recall.
Root cause
Other
Status
Terminated
Product code
FRN
Distribution
Product was distributed nationwide to 746 domestic consignees. Product was distributed internationally to the following countries: Puerto Rico, Canada, Saudi Arabia, Taiwan, Australia, Italy, Jordan,
Date initiated
2005-05-18
Date posted
2006-01-12
Date terminated
2006-12-21
Location
Morgan Hill, CA

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