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BeneVision Series Telemetry Monitor. Operators Manuals: TM70 TM80

Official notice

14 Oct 2026

Last checked

20 Oct 2026

LowFDA

An official FDA notice concerns Mindray Ds. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2026-10-14. Recall numbers: Z-0111-2027. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

29,737

Recall number

Z-0111-2027

Official notice

2026-10-14

The hazard

Health risk requiring medical assessment

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

99828

Recall Numbers

Z-0111-2027

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Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States

Affected area 1

US · United States

Affected area 2

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Mindray Ds. Contact: Mindray DS USA, Inc..

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class III

App estimate

low

Recall details

Recall number

Z-0111-2027

Event id

99828

Units affected

29,737

Status

active

Classification

Class III

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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