Medtronic Neuromodulation Medtronic InterStim Ground Pad REF 041826 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic InterStim Ground Pad REF 041826
Brand
Medtronic Neuromodulation
Lot Codes / Batch Numbers
Product Number: 041826, UDI: 20763000343273, Lot Number: 60347246
Products Sold
Product Number: 041826; UDI: 20763000343273; Lot Number: 60347246
Medtronic Neuromodulation is recalling Medtronic InterStim Ground Pad REF 041826 due to Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.
Recommended Action
Per FDA guidance
The consignee recall notification was sent out via mail on 07/06/2023. The letter instructs the consignee to return any affected product they may have, and to forward the notification to those who need to be aware within the organization or to any location which the devices have been transferred. Consignee also asked to complete and return a confirmation.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026