Fresh Recalls

Mindray DS USA recalls

8 recent recalls on record for Mindray DS USA in connected official government data as of October 22, 2026 at 12:00 PM UTC.

Models with recalls

BeneView Series (1)BeneVision N1 and N-Series Patient Monitor (1)BeneVision Series Telemetry Monitor (1)Panorama and Telemetry Monitoring System (1)Passport Series Patient Monitor (1)T1 Patient Monitor (1)cPM Series Patient Monitor (1)ePM Series Patient Monitor (1)

All Mindray DS USA recalls

FDA Class III · Medical device · October 14, 2026

T1 Patient Monitor recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0116-2027 · Official record ↗

FDA Class III · Medical device · October 14, 2026

cPM Series Patient Monitor recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0115-2027 · Official record ↗

FDA Class III · Medical device · October 14, 2026

Passport Series Patient Monitor recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0114-2027 · Official record ↗

FDA Class III · Medical device · October 14, 2026

BeneView Series recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0113-2027 · Official record ↗

FDA Class III · Medical device · October 14, 2026

Panorama and Telemetry Monitoring System recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0112-2027 · Official record ↗

FDA Class III · Medical device · October 14, 2026

BeneVision Series Telemetry Monitor recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0111-2027 · Official record ↗

FDA Class III · Medical device · October 14, 2026

BeneVision N1 and N-Series Patient Monitor recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0110-2027 · Official record ↗

FDA Class III · Medical device · October 14, 2026

ePM Series Patient Monitor recall — Mindray DS USA, Inc.

Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions

Official ID Z-0109-2027 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.