Lower riskMedical device recall · FDA · Published May 27, 2021
Mindray BeneVision TD60 Telepack Battery Cradle May Not Power On
Mindray recalls 3AA battery cradles for BeneVision TD60 and TM80 Telepacks that may not power on properly. Affected units include specific model numbers and part numbers.
“Mindray BeneVision TD60 Telepack Battery Cradle May Not Power On.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62467-mindray-benevision-td60-telepack-battery-cradle-may-not-power-on. Based on FDA recall #Z-2108-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2108-2021%22&limit=1).
Mindray DS USA, Inc. dba Mindray North America recalled 3AA battery cradles used with BeneVision TD60 and TM80 Telepacks due to a potential power-on failure, the FDA said on May 27, 2021.
How to tell if you have it
Brand: Mindray
Product: 3AA battery cradle (Part Number 045-001699-01)
Compatible with BeneVision TD60 Telepack (Model Number 115-047566-00 / 115-060044-00)
Compatible with TM80 Telepack (Model Number 115-047565-00 / 120-018867-00)
Units affected: 804
Distribution: US nationwide and Canada
The hazard
The telepack may not power on when using the 3AA battery cradle, according to the FDA.
Context
GovInfoNow's records show Mindray DS USA, Inc. dba Mindray North America has 13 other recalls on record since July 14, 2017. Other recent recalls of similar products include Mindray BeneVision Distributed Monitoring: Audio Failure Risk (Nov. 18, 2025), Mindray Isoflurane V90 Vaporizer Recall (Oct. 20, 2025), and Mindray BeneVision N1 Patient Monitor Recall (Aug. 15, 2025). Other recent recalls of similar products include HeartMate 11V Backup Battery Recall (May 13, 2026).
How to tell if you have this one
Check for the part number 045-001699-01 on the battery cradle. The cradle is used with BeneVision TD60 Telepack (model numbers 115-047566-00 or 115-060044-00) or TM80 Telepack (model numbers 115-047565-00 or 120-018867-00).
Brand
Mindray
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Battery Cradle Part Number
Look for part number 045-001699-01 on the battery cradle.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Distributed US nationwide and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2108-2021 (May 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2108-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.