Z-2365-2023 Class II Ongoing
FDA device recall Z-2365-2023 was initiated by Medtronic Neuromodulation on Jul 6, 2023 and is designated Class II. Reason for recall: Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date. The recall status is ongoing. Affected quantity: 360 packs (36 kits of 10 packs each).
Recall Details
- Product Type
- Devices
- Report Date
- Aug 16, 2023
- Initiation Date
- Jul 6, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 360 packs (36 kits of 10 packs each)
Product Description
Medtronic InterStim Ground Pad REF 041826
Reason for Recall
Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.
Distribution Pattern
International distribution to the country of Iran.
Code Information
Product Number: 041826; UDI: 20763000343273; Lot Number: 60347246
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2365-2023
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026