Recall Z-0518-2021— Medtronic Inc.

Name: FDA recall Z-0518-2021
Creator: U.S. Food and Drug Administration
Published: 2020-04-30

Class II · Ongoing

Class II FDA medical device recall by Medtronic Inc., initiated 2020-04-30. FDA's recall record names no specific 510(k) clearance for this event. Product: MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.. Reason: Missing solder battery connection, which could interrupt power of insulin pump..

Recalling firm: Medtronic Inc.
Classification: Class II
Status: Ongoing
Initiated: 2020-04-30
Firm location: Northridge, CA, United States

Product description

MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.

Reason for recall

Missing solder battery connection, which could interrupt power of insulin pump.

Data sourced from openFDA. This site is unofficial and independent of the FDA.