FDA Recall Terminated

CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates sensor data and provides reports of continuous glucose information

Recall: Z-1501-2016 · Initiated February 19, 2016

Recall

Recall Number
Z-1501-2016
Event Number
73451
Firm
Medtronic MiniMed Inc.
FEI Number
3003166194
Product Code
OUG
Status
Terminated
Root Cause
Employee error
Initiated
February 19, 2016
Terminated
May 16, 2016
Address
18000 Devonshire St, Northridge, CA, 91325-1219

Description

CareLink iPro2 Reports, Model No. MMT-7340 is software intended to retrospectively calibrates sensor data and provides reports of continuous glucose information

Reason

Medtronic MiniMed is recalling 19 CareLink iPro Therapy Management reports because the CareLink iPro reports were created using the Pacific Standard Time zone as the time reference, although the patients and their sensor data were subject to the Central Standard Time zone. The CareLink iPro2 Professional CGM (continuous glucose monitor) data uploading error that resulted in an inaccurate time zone being applied to 19 CareLink iPro reports.

Action

An Urgent Field Safety Notice was sent to customers on 2/19/16 to make customers aware of an iPro2 Professional CGM (continuous glucose monitor) data uploading error that resulted in an inaccurate time zone being applied to 21 CareLink iPro reports. The letter informs customers that the affected CareLink iPro reports were created using the Pacific Standard Time zone as the time reference, although the patients and their sensor data were subject to the Central Standard Time zone. The letter informs the customers of the requested next steps and to contact Maneesh Shrivastav, Director of Strategy at Medtronics Diabetes by email at [email protected] or call (763) 526-3509 if they have any questions.

Distribution

US: MN

Quantity

20