Reported Mar 6, 2024 · Ongoing

Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, REF 46917, Sterile…

Medtronic Neurosurgery

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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 Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, REF 46917, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce intracranial pressure and CSF volume.
Lot codes and dates
  • Lot Number/GTIN
    • 222277587 00613994445407
    • 223565027 00763000624804
    • 223580362 00763000624804
    • 223698572 00763000624804
    • 223734523 00763000624804
    • 223999040 00763000406028
    • 224301720 00763000406028
    • 224302820 00613994445407
    • 224973997 00613994445407
    • 224990852 00613994445407
    • 224990870 00613994445407
    • 224990871 00613994445407
    • 225198822 00613994445407
    • 226490967 00763000624804
    • 226517899 00763000624804
    • 226546799 00613994445407
    • 226571115 00613994445407
    • 226665388 00763000624804
    • 226665395 00613994445407
    • 226734688 00763000624804
    • 226734689 00763000624804
    • 226756273 00763000406028
Amount recalled
3, 889 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

Stop using this product now

Potential for catheter disconnection from the patient line stopcock connectors.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 7:40 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.