FDA-Device2023-08-23Class II
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Medtronic Neurosurgery
Hazard
Product labeling contains incorrect expiration date
Sold states
US Nationwide distribution in the states of NJ, FL, CA, IL.
Affected count
44 units
Manufactured in
5290 California Ave, Irvine, CA, United States
Products
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2412-2023Don't want to check this manually?
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