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

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 — recall Z-2680-2017

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

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2680-2017
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): 14040001

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.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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.

Related