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

Recall Z-1942-2012 — Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange. Philips Xcelera Connect R2.x is a generic interface and data mapping engine between a Hospital Information System (HIS), Imaging Modalities, Xcelera PACS and Xcelera Cath Lab Manager (CLM). This interface engi

U.S. FDA — Device Enforcement · United States · 2012-06-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1942-2012
Date of alert: 2012-06-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Philips Healthcare Inc.
Product category: device
Product type: Devices

Reported risk: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from unformatted reports interface

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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