Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Recalled by Mindray DS USA, Inc. dba Mindray North America Due to Telepack may not power on when using the...

Date: May 27, 2021
Company: Mindray DS USA, Inc. dba Mindray North America
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Mindray DS USA, Inc. dba Mindray North America directly.

Affected Products

3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Telepack (Model Number 115-047565-00 / 120-018867-00). Used with physiological data monitor.

Quantity: 804

Why Was This Recalled?

Telepack may not power on when using the 3AA battery cradle.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Mindray DS USA, Inc. dba Mindray North America

Mindray DS USA, Inc. dba Mindray North America has 39 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report