Gastrointestinal Imaging Video Capsule Device (2019-07-18)

Starting date:

July 18, 2019

Posting date:

August 23, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-70769

Last updated: 2019-09-17

• Reason
• Affected products

Affected Products

Gastrointestinal Imaging Video Capsule Device

Reason

Possible mislabelling/mismatching with incorrect serial number linked to patient data.

Affected products