Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2873-2016 — LifeCare PCA Infusion System with Hospira MedNet Software, PCA Serial List Number 20709 Allows for clinician administration or self-administration of analgesic medications.

U.S. FDA — Device Enforcement · United States · 2013-03-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2873-2016
Date of alert
2013-03-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hospira Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
15553367
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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