Overview of recall records associated with Mindray DS USA, Inc. d.b.a. Mindray North America, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Mindray has identified a software anomaly that may where, in the presence of an asystole, the Telepack ECG waveform may produce a unique step pattern (instead of a flat line) if Lead 1 or V…
Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.
This page summarizes recall records in which the official source identifies Mindray DS USA, Inc. d.b.a. Mindray North America as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
