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Medical Device

cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12

Recall date: 2026-10-14 · Source: FDA_DEVICE
Brand / Firm
Mindray DS USA, Inc.
Product
cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12
Reason for recall
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Units affected
1,699 units
Description
cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12
View official recall notice →