Mindray DS USA, Inc. dba Mindray North America 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Mindray DS USA, Inc. dba Mindray North America
Lot Codes / Batch Numbers
Part Number 045-001699-01, Awaiting additional details
Products Sold
Part Number 045-001699-01; Awaiting additional details
Mindray DS USA, Inc. dba Mindray North America is recalling 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115- due to Telepack may not power on when using the 3AA battery cradle.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Telepack may not power on when using the 3AA battery cradle.
Recommended Action
Per FDA guidance
Urgent Medical Device Correction notification letters dated 5/27/21 were sent to customers. Actions to be taken by the Customer/User Please discard all 3AA battery cradles in stock that were purchased between October 1, 2020 and March 31, 2021. Shipping records indicate your facility has XX cradles affected by this recall. Continue to use the TD60 and TM80 telepacks normally with either the 2AA battery cradle (TD60 only), or rechargeable Li-ion battery pack, if previously purchased. Please complete and return the Acknowledgement and Receipt form (found on the 3rd page of this recall notice) by June 30, 2021. Product and Distribution Information The 3AA cradles included with the TD60 or TM80 telepacks distributed between October 1, 2020 and March 31, 2021 may be affected by this recall. Other Information Please complete the attached Acknowledgement and Receipt Form and return in the stamped envelope provided. Contact information is provided below should you have questions. Adverse reactions or quality problems experienced with the use of this product may be reported to FDAs MedWatch Adverse Event Reporting program either online, by regular mail or by fax. We apologize for any inconvenience this may cause and appreciate your cooperation. Sincerely, Diane Arpino Director, Quality Operations and Regulatory Affairs Mindray DS USA, Inc. d.arpino@mindray.com 201.995.8407 Distributors were instructed to do the following: Actions to be taken by the Customer/User Please discard all 3AA battery cradles in stock that were purchased between October 1, 2020 and March 31, 2021. Shipping records indicate your facility purchased 6 cradles affected by this recall. Continue to use the TM80 telepack normally with rechargeable Li-ion battery pack, if previously purchased. Please contact each customer which you have distributed the affected 3AA battery cradles. The format for the recall notification to send to your customers is provided. We recommend that you send the notificati
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026