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Hospira Inc. recalls LifeCare PCA 3, PCA Serial List Number 12384 Allows for clinician administration or self-administration of analgesic
Recalled September 28, 2016 · FDA recall Z-2874-2016 · Hospira
Hazard
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. · FDA Class II
Units
69
Sold at
United States (Nationwide) Distribution including Puerto Rico and American Virgin Islands.
Description
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.
Product
LifeCare PCA 3, PCA Serial List Number 12384 Allows for clinician administration or self-administration of analgesic medications.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →