Reported Aug 23, 2023 · Ongoing

Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter,…

Medtronic Neurosurgery

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medtronic Neurosurgery · 5290 California Ave · Irvine, CA · 92617-3073

Is this the product you have?

  • Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
Lot codes and dates
  • Lot # 226632942
  • UDI-DI00763000624781
Amount recalled
44 units

Where it was sold

Why it was recalled

Product labeling contains incorrect expiration date

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:13 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.