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

Recall Z-0288-2014 — The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+3 Infusion System is designed to deliver parenteral, enteral, or epidural infusions over a broad range

U.S. FDA — Device Enforcement · United States · 2013-02-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0288-2014
Date of alert
2013-02-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hospira Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
14040001
Reported risk: Plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure sensor pin is a part of the overall subsystem that measures the pressure within the distal line of the administration set and indicates the presence of a full or partial distal occlusion. A broken distal pin can only be detected via a visual inspection of the distal pressure pin. A broken
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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