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

Recall Z-0624-2013 — Plum A+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold under the following configurations: a) list 11971; b) list 11973 - software version 10.3; c) list 12391 - software version 11.3; d) list 20679 - Hospira MedNet Software e) list 20792 - Hospira MedNet Sof

U.S. FDA — Device Enforcement · United States · 2012-12-07 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0624-2013
Date of alert: 2012-12-07
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hospira Inc.
Product category: device
Product type: Devices

Reported risk: The door roller assembly on the Plum A+/A+3 infuser family of infusers has the potential to break which can lead to possible unrestricted flow and/or over-delivery during the removal of the IV administration set's cassette from the pump.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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