Mindray DS USA, Inc. dba Mindray North America: Medical Device Recall in 2021 - (Recall #: Z-2108-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class III

Date Initiated: May 27, 2021

Date Posted: July 28, 2021

Recall Number: Z-2108-2021

Event ID: 88209

Reason for Recall:

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

Status: Terminated

Product Quantity: 804

Code Information:

Part Number 045-001699-01; Awaiting additional details

Distribution Pattern:

Distributed US nationwide and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated