PlainRecalls
FDA Devices Moderate Class II Terminated

LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-administration of analgesic medications.

Reported: September 28, 2016 Initiated: March 8, 2013 #Z-2873-2016

Product Description

LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-administration of analgesic medications.

Reason for Recall

Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this malfunction occurs, the pump will alarm and infusion stops.

Details

Recalling Firm
Hospira Inc.
Units Affected
8,794
Distribution
United States (Nationwide) Distribution including Puerto Rico and American Virgin Islands.
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-administration of analgesic medications.. Recalled by Hospira Inc.. Units affected: 8,794.
Why was this product recalled?
Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this malfunction occurs, the pump will alarm and infusion stops.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 28, 2016. Severity: Moderate. Recall number: Z-2873-2016.