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

Recall Z-1073-2015 — The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environments. It is a cassette based multi-function infusion system. The Plum A+ allows two lines in and one line out. The pump can be used for standard, piggyback, or concurrent delivery.

U.S. FDA — Device Enforcement · United States · 2014-07-02 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1073-2015
Date of alert: 2014-07-02
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Hospira Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 15867001

Reported risk: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may fail to sound at all volume levels.

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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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