BEMER Therapy System (2021-01-06)

Starting date:

January 6, 2021

Posting date:

January 15, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-74761

Last updated:
2021-01-15

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  Reason
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  Affected products

Affected Products 

A. BEMER Pro Therapy System

B. BEMER Classic Therapy System

Reason

Recall due to correction to inform customers of the additional contraindication related to active medical implants and implants intended for drug delivery (e.g., drug pumps), the use of the BEMER therapy system could lead to malfunctions in these devices.

Affected products