Medtronic MiniMed(TM) Pro-set(TM) recall
Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
Why was Medtronic MiniMed(TM) Pro-set(TM) recalled?
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Lot Numbers: 6211649, 6207537
- Product
- Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)
- Recalling firm
- Medtronic Inc.
- Quantity
- 5,842 units
- Distribution
- Worldwide
- Recall date
- November 29, 2017
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)