# Mindray DS USA, Inc. recall opens medical devices buyers to alternatives (2026-10-14)

**Switch Opportunity Score:** 25/100

| Field | Value |
|---|---|
| Recalling firm | Mindray DS USA, Inc. |
| Product | BeneView Series. Operator's Manuals: T5 / T8 |
| Replacement market | Medical devices |
| Agency | FDA medical devices |
| Severity | standard |
| Hazard | Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions |
| Recall date | 2026-10-14 |
| Switch angle | Buyers and retailers of the recalled medical devices need a compliant replacement; position your product on the specific hazard fixed, with documentation. |
| Original recall record | /report/fdapulse/z-0113-2027 |

## Why this score


Source: CPSC, NHTSA and FDA device recalls (via our recall feeds), mapped to replacement markets (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0113-2027%22). Last refreshed: 2026-11-04T15:17:38.587Z.
Built from official CPSC, NHTSA and FDA recall data; market mapping is our classification. Do not make claims about a competitor's recall beyond what the agency published, and follow advertising and comparative-claims rules. Not a consumer report and may not be used for FCRA purposes. Informational only; not legal, investment or procurement advice. Not affiliated with any agency or company listed.