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

Recall Z-2683-2017 — The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel

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-2683-2017
Date of alert: 2013-02-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: ICU
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 16061001

Reported risk: A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.

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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