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

Recall Z-0374-2016 — Philips IntelliVue Information Center iX (release A.00, A.01, and A.02) are impacted by this issue: 866023 IntelliVue Info Center iX 866024 PIIC iX Upgrade 866117 PIIC Classic Upgrade The intended use of the Information Center Software is to display physiologic waves, parameters, and trends, f

U.S. FDA — Device Enforcement · United States · 2014-12-19 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0374-2016
Date of alert: 2014-12-19
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Philips Medical Systems, Inc.
Product category: device
Product type: Devices

Reported risk: Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled without visual notification

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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