Recall Z-2603-2017— Medtronic Inc.
Class II · Terminated
Class II FDA medical device recall by Medtronic Inc., initiated 2017-05-08, terminated 2021-01-20. FDA's recall record names no specific 510(k) clearance for this event. Product: MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.. Reason: Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive..
- Recalling firm
- Medtronic Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2017-05-08
- Terminated
- 2021-01-20
- Firm location
- Northridge, CA, United States
Product description
MiniMed 630G Insulin Infusion Pump, Catalog No. MMT-1715, MMT-1755.
Reason for recall
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
Data sourced from openFDA. This site is unofficial and independent of the FDA.