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

Recall Z-0630-2013 — DPM Central Station Mindray DS USA, Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 The Central Monitoring Station (CMS) network transfers information between DOM Central Station and other network devices. It also allows information transfer between several CMS. Network connections consist of har

U.S. FDA — Device Enforcement · United States · 2011-05-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0630-2013
Date of alert: 2011-05-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Mindray DS USA, Inc. d.b.a. Mindray North America
Product category: device
Product type: Devices

Reported risk: There is a software anomaly with the DPM Central Monitoring System where the trend data of one patient maybe replaced with the trend data of a second patient.

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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