Recall Ledger

Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama... recall (Mindray DS USA, Inc.)

Medical deviceClass IIIOngoing

Summary: Mindray DS USA, Inc. is recalling Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60).. Reason: Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions.

What is being recalled

Panorama and Telemetry Monitoring System. Operator's Manuals: TMS-6016/Panorama Telepack-608/TMS60 (TD60).

Why

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

How serious is it

Class III is the least serious level: using or being exposed to this product is not likely to cause health problems, but it breaks FDA rules.

Where it was sold

Worldwide - Nationwide and the country of Canada.

How to tell if yours is affected

Part Numbers of the Panorama and Telemetry Monitoring System Operator's Manuals: 1. Panorama Telepack-608 Telemetry Monitoring System Operator's Manual up to and including revision 1.0; Part No. 046-007526-00 2. TMS-6016 Operator's Manual up to and including revision 11.0; Part No. 046-005012-00

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-0112-2027
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass III
StatusOngoing
Recall startedAugust 31, 2026
ReportedOctober 14, 2026
CompanyMindray DS USA, Inc.
Company locationMahwah, NJ, United States
Initiated byVoluntary: Firm initiated
Quantity11,831 units

More recalls from Mindray DS USA, Inc. · all medical device recalls · recalls from August 2026

Official FDA record