Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2365-2023 — Medtronic InterStim Ground Pad REF 041826

U.S. FDA — Device Enforcement · United States · 2023-07-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2365-2023
Date of alert
2023-07-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Neuromodulation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20763000343273
Reported risk: Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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