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.
Reported: July 28, 2021 Initiated: May 27, 2021 #Z-2108-2021
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.
Reason for Recall
Telepack may not power on when using the 3AA battery cradle.
Details
- Recalling Firm
- Mindray DS USA, Inc. dba Mindray North America
- Units Affected
- 804
- Distribution
- Distributed US nationwide and Canada.
- Location
- Mahwah, NJ
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Mindray DS USA, Inc. dba Mindray North America. Units affected: 804.
Why was this product recalled? ▼
Telepack may not power on when using the 3AA battery cradle.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 28, 2021. Severity: Low. Recall number: Z-2108-2021.
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