FDA recall record

Mindray DS USA, Inc. dba Mindray 3AA battery cradle recall — FDA Z-2108-2021

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

Class IIIclassification
Z-2108-2021official record ID
Jul 28, 2021report date

Recall record at a glance

Official recordZ-2108-2021
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmMindray DS USA, Inc. dba Mindray North America
Report dateJul 28, 2021
Recall initiation dateMay 27, 2021
Quantity804
LocationMahwah, NJ, United States

Official 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.

Why the product was recalled

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

Distribution information

Distributed US nationwide and Canada.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.