FDA recall Z-2365-2023

Medtronic Neuromodulation · Class II · device

Product

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

International distribution to the country of Iran.

Key facts

Status
Ongoing
Initiation date
2023-07-06
Report date
2023-08-16
Voluntary/Mandated
Voluntary: Firm initiated
Location
Minneapolis, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2365-2023