FDA recall Z-2412-2023

Medtronic Neurosurgery · Class II · device

Product

Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only

Reason for recall

Product labeling contains incorrect expiration date

Distribution

US Nationwide distribution in the states of NJ, FL, CA, IL.

Key facts

Status
Ongoing
Initiation date
2023-06-28
Report date
2023-08-23
Voluntary/Mandated
Voluntary: Firm initiated
Location
Irvine, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2412-2023