Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic REF 46915 Duet External Drainage and Monitoring system Recalled by Medtronic Neurosurgery Due to Product labeling contains incorrect expiration date
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Neurosurgery directly.
Affected Products
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Quantity: 44 units
Why Was This Recalled?
Product labeling contains incorrect expiration date
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Neurosurgery
Medtronic Neurosurgery has 31 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report