Mindray DS USA Passport Series Patient Monitor recall — FDA Z-0114-2027
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Overview of recall records associated with Mindray DS USA, Inc., including dates, categories and classifications where available.
Classification mix: Class III: 1.
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
This page summarizes recall records in which the official source identifies Mindray DS USA, Inc. 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.