Medtronic Neurosurgery: Medical Device Recall in 2023 - (Recall #: Z-2412-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 28, 2023

Date Posted: August 23, 2023

Recall Number: Z-2412-2023

Event ID: 92702

Reason for Recall:

Product labeling contains incorrect expiration date

Status: Ongoing

Product Quantity: 44 units

Code Information:

Lot # 226632942; UDI-DI: 00763000624781

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated