Recall Z-0115-2027 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Mindray DS USA, Inc.
cPM Series Patient Monitor. Operator's Manual: cPM 8/cPM 12
| Date | Oct 7, 2026 (initiated Aug 31, 2026) |
| Status | Open, Classified |
| Reason | Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions |
| Root cause | Labeling design |
| Action | Mindray 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 |
| Quantity | 1,699 units |
| Distribution | Worldwide - Nationwide and the country of Canada. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K153448 | Passport Series Patient Monitors (Including Passport 8, Passport 12) Shenzhen Mindray Bio-Medical Electronics Co., Ltd., Mar 3, 2016 |