# FDA recall Z-2412-2023

> **Medtronic Neurosurgery** · Class II · device recall initiated 2023-06-28.

## 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

- **Recall number:** Z-2412-2023
- **Recalling firm:** Medtronic Neurosurgery
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-28
- **Report date:** 2023-08-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irvine, CA, United States

## Primary source

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

## Citation

> AI Analytics. FDA recall Z-2412-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2412-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*