Recall Z-1355-2022— Medtronic MiniMed
Class II · Ongoing
Class II FDA medical device recall by Medtronic MiniMed, initiated 2022-05-23. FDA's recall record names no specific 510(k) clearance for this event. Product: MiniMed 670G Insulin Pump (U.S. and O.U.S. Version). Reason: Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps..
- Recalling firm
- Medtronic MiniMed
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-05-23
- Firm location
- Northridge, CA, United States
Product description
MiniMed 670G Insulin Pump (U.S. and O.U.S. Version)
Reason for recall
Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps.
Data sourced from openFDA. This site is unofficial and independent of the FDA.