FDAClass IIOctober 5, 2016

CareLink iPro Version 1.10 recall: Software Issue

CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, the CareLink iPro software…

Why was CareLink iPro Version 1.10 recalled?

Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

n/a

Product
CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, the CareLink iPro software…
Recalling firm
Medtronic Inc.
Quantity
33 units
Distribution
Nationwide Distribution to TN, MN, and WA
Recall date
October 5, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
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