PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: August 23, 2023 Initiated: June 28, 2023 #Z-2412-2023

Product Description

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

Details

Recalling Firm
Medtronic Neurosurgery
Units Affected
44 units
Distribution
US Nationwide distribution in the states of NJ, FL, CA, IL.
Location
Irvine, CA

Frequently Asked Questions

What product was recalled?
Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only. Recalled by Medtronic Neurosurgery. Units affected: 44 units.
Why was this product recalled?
Product labeling contains incorrect expiration date
Which agency issued this recall?
This recall was issued by the FDA Devices on August 23, 2023. Severity: Moderate. Recall number: Z-2412-2023.