Lower riskMedical device recall · FDA · Published June 28, 2023
Medtronic Duet Drainage System Has Incorrect Expiration Date Label
Medtronic recalls Duet External Drainage and Monitoring system with incorrect expiration date labeling. Affected units may have safety risks due to outdated expiration dates.
“Medtronic Duet Drainage System Has Incorrect Expiration Date Label.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57771-medtronic-duet-drainage-system-has-incorrect-expiration-date-label. Based on FDA recall #Z-2412-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2412-2023%22&limit=1).
The FDA announced on June 28, 2023, that Medtronic Neurosurgery is recalling the REF 46915 Duet External Drainage and Monitoring system due to incorrect expiration date labeling. The agency issued recall number Z-2412-2023 for the Class II voluntary recall.
The product labeling contains an incorrect expiration date. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Medtronic Neurosurgery has 9 other recalls on record since December 20, 2017. Other recent recalls of similar products include Medtronic Ventriculostomy Kit Recall (June 17, 2026), Medtronic Exacta External Drainage System recall (November 1, 2024), and Medtronic Duet Drainage System recall (January 22, 2024). Other recent recalls of similar products include BD Ready-to-Use Hydrophilic Catheter 14 Fr (November 29, 2025) and Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation (May 13, 2026).
How to tell if you have this one
Check for the lot number 226632942 and UDI-DI code 00763000624781 on the product packaging. This system is sold as a sterile, prescription-only device for medical use.
Brand
Medtronic Neurosurgery
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the lot number 226632942 and UDI-DI code 00763000624781 on the product packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 4 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of NJ, FL, CA, IL.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, Illinois, New Jersey.
Recall timeline
FDA published this recall 56 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2412-2023 (June 28, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2412-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.