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