Health product recall

MiniMed Mio Advance (2018-12-18)

Starting date:
December 18, 2018
Posting date:
January 11, 2019
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-68746

Affected products

MiniMed Mio Advance

Reason

An increase of subcutaneous infusion of insulin, which could lead to over-delivery of insulin to the patient.

Affected products

MiniMed Mio Advance

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

MMT-212600

MMT-233600

MMT-242600

MMT-242T

MMT-247600

MMT-247T

MMT-248600

Companies
Manufacturer

Unomedical A/S

Aaholmvej 1-3

Osted, Lejre

DENMARK