Medtronic Australasia Pty Ltd — CareLink (CL) Software and CL System using CareLink Reports

PRA number

2020/18708

Published date

Product description

CareLink (CL) software and CL System using CareLink reports
Versions: v14.1a, v3.1a and v5.2b

Product codes: MMT-7333, MMT-7350 and ACC-7333

ARTG 303062
(Medtronic Australasia Pty Ltd - Information system)

Reasons the product is recalled

Following an update to CareLink software on 29 August, 2020, consumers who generated a report from CareLink Personal or CareLink system software may have been presented with an inaccurate carbohydrate ratio setting on their CareLink report.

This only occurred under the following circumstances:
1. The carbohydrate unit of measurement in CareLink software is set to grams, but the insulin pump is set to exchanges.
2. The carbohydrate unit of measurement in CareLink software is set to exchanges, but the insulin pump is set to grams.



The hazards to consumers

If adjustments were made to the carbohydrate ratio based on the CareLink report, this could lead to either over or under delivery of insulin. This could cause low blood glucose (hypoglycemia, loss of consciousness, seizure, death), and/or high blood glucose (hyperglycemia) which can lead to serious health complications.

What consumers should do

Medtronic will contact affected users in writing. Consumers who may have adjusted their carbohydrate ratio between 29 August 2020 and 30 September 2020 using incorrect data on the CareLink report, should review their carbohydrate ratio setting with a healthcare provider to determine if any corrections are needed and should discard and re-generate the Carelink report.

On 30 September 2020, Medtronic released an automatic update to CareLink software which resolved the issue described. No further action is required to receive the corrected version of CareLink software.

For further information, please contact Medtronic Customer Service by phone on 1800 777 808.

Where the product was sold

Nationally
International

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category

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