medical LOW RISK Updated 2026-10-14

Mindray DS USA, Inc. recalls BeneView Series. Operator's Manuals: T5 / T8

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Recalled Product

BeneView Series. Operator's Manuals: T5 / T8

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Part Numbers of the BeneView Series Operator's Manuals: 1. BeneView T5 Operator's Manual up to and including revision 17.0; Part No. 6802-20-66856 2. BeneView T8 Operator's Manual up to and including revision 16.0; Part No. 6800-20-50710

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
View official government recall