Recall archive / FDA device enforcement
Medtronic InterStim Ground Pad REF 041826 — FDA record Z-2365-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jul 6, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Medtronic InterStim Ground Pad REF 041826
- Reason
- Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.
- Classification
- Class II
- Recalling firm
- Medtronic Neuromodulation
- Quantity
- 360 packs (36 kits of 10 packs each)
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2365-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Product Number: 041826; UDI: 20763000343273; Lot Number: 60347246 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
International distribution to the country of Iran.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Aug 16, 2023
- Recall initiation date
- Jul 6, 2023
- Center classification date
- Aug 10, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.