MiniMed 630G & 670G Insulin Pump (2020-05-01)
- Starting date:
- May 1, 2020
- Posting date:
- May 15, 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-73121
Last updated: 2020-05-15
Affected Products
- MiniMed 630G Insulin Pump
- MiniMed 670G Insulin pumps
Reason
The MiniMed 600 Series insulin pump uses an AA battery for power. Recently, manufacturer identified a batch of pumps with an issue on the battery connection that does not meet quality specifications. If power is interrupted on a patient's insulin pump, then insulin is suspended which may lead to hyperglycemia (high blood sugar). There have been no reported complaints from customers as a result of this issue
Affected products
A. MiniMed 630G Insulin Pump
Lot or serial number
- More than 10 numbers, contact manufacturer.
Model or catalog number
- MMT-1714K
Companies
- Manufacturer
-
Medtronic Minimed
18000 Devonshire St.
Northridge
91325
California
UNITED STATES
B. MiniMed 670G Insulin pumps
Lot or serial number
- More than 10 numbers, contact manufacturer.
Model or catalog number
- MMT-1782K
Companies
- Manufacturer
-
Medtronic Minimed
18000 Devonshire St.
Northridge
91325
California
UNITED STATES