NEEVA BABY FETAL DOPPLER (2020-08-02)

Starting date:

August 2, 2020

Posting date:

November 20, 2020

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-74347

Last updated: 2020-11-19

• Reason
• Affected products

Affected Products

NEEVA BABY FETAL DOPPLER

Reason

The device was not licensed under the manufacturer name at the moment of the sale.

Affected products