Recall Z-2365-2023— Medtronic Neuromodulation

Name: FDA recall Z-2365-2023
Creator: U.S. Food and Drug Administration
Published: 2023-07-06

Class II · Ongoing

Class II FDA medical device recall by Medtronic Neuromodulation, initiated 2023-07-06. FDA's recall record names no specific 510(k) clearance for this event. 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..

Recalling firm: Medtronic Neuromodulation
Classification: Class II
Status: Ongoing
Initiated: 2023-07-06
Firm location: Minneapolis, MN, United States

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.