Medtronic MiniMed Inc.: Medical Device Recall in 2016 - (Recall #: Z-1501-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: February 19, 2016

Date Posted: April 27, 2016

Recall Number: Z-1501-2016

Event ID: 73451

Reason for Recall:

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.

Status: Terminated

Product Quantity: 20

Code Information:

n/a

Distribution Pattern:

US: MN

Voluntary or Mandated:

Voluntary: Firm initiated