FDAClass IIAugust 16, 2023

Medtronic InterStim Ground Pad recall

Medtronic InterStim Ground Pad REF 041826

Why was Medtronic InterStim Ground Pad recalled?

Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.

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?

Product Number: 041826; UDI: 20763000343273; Lot Number: 60347246

Product
Medtronic InterStim Ground Pad REF 041826
Recalling firm
Medtronic Neuromodulation
Quantity
360 packs (36 kits of 10 packs each)
Distribution
International distribution to the country of Iran.
Recall date
August 16, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls