ClearanceBrief
Recall Z-0111-2027 ยท MSX System, Network And Communication, Physiological Monitors

Mindray DS USA, Inc.

BeneVision Series Telemetry Monitor. Operator's Manuals: TM70/TM80

DateOct 7, 2026 (initiated Aug 31, 2026)
StatusOpen, Classified
ReasonCertain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
Root causeLabeling design
ActionMindray notified consignees on about 08/31/2026 via "URGENT: Medical Device Recall" letter. Consignees were informed that Mindray was providing updated instructions regarding physiological alarms in certain Mindray patient monitoring device Instructions for Use (IFU)/Operator s Manuals. This action is limited to updates to the IFU/Operators Manual content and does not require removal, return, repair, or replacement of the monitors. Consignees were instructed to continue using the Mindray monitors associated with the affected operator s manual, ensure that applicable clinical staff are made
Quantity29,737 units
DistributionWorldwide - Nationwide and the country of Canada.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K242728BeneVision Central Monitoring System
Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Jul 31, 2025