Reported Mar 6, 2024 · Ongoing
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…
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, REF 46913, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce intracranial pressure and CSF volume.
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Barcodes Product as published 22227412500613994445360222322811 00763000406004; 222322812 00763000406004; 222322813 00763000406004; 222580925 00763000406004; 223564705 00763000624767; 223659557 00763000624767; 223659558 00763000624767;; 223734520 00763000624767; 223778508 00763000624767; 223818450 00763000624767; 223999039 00763000406004; 224032596 00763000406004; 224197127 00763000406004; 224218026 00763000406004; 224218028 00763000406004; 224255795 00763000406004; 224277483 00763000406004; 224302821 00763000406004; 224333656 00613994445360; 224878533 00763000624767; 224918533 00763000406004; 224918534 00763000624767; 224918535 00763000624767; 224918536 00763000624767; 224949836 00763000406004; 224949837 00763000406004; 224973998 00763000624767; 224973999 00763000624767; 224990662 00763000406004; 224990663 00763000624767; 224990848 00763000406004; 224990849 00763000624767; 224990850 00763000624767; 224990867 00763000624767; 224990868 00763000624767; 224990886 00763000624767; 225035261 00763000406004; 225234318 00763000406004; 225279760 00763000406004; 225336442 00613994445360; 225336443 00613994445360; 225375797 00763000406004 22537579800763000406004225419717 00763000406004; 225422438 00763000406004; 225468101 00613994445360; 225558567 00763000406004; 225559817 00763000406004 22555981800763000406004225587869 00763000406004; 225587870 00763000406004; 225749838 00763000406004; 226091713 00763000406004; 226111273 00763000406004; 226242270 00763000624767; 226242271 00763000624767; 226288880 00763000624767; 226335061 00763000406004; 226335062 00763000624767; 226467306 00763000624767 22649096600763000624767226517895 00763000624767; 226517896 00763000624767; 226517900 00763000406004; 226546791 00763000624767; 226546794 00763000624767; 226571112 00763000624767; 226571113 00763000624767; 226650893 00763000624767; 226650894 00763000624767; 226665390 00763000406004; 226665391 00763000406004; 226665392 00763000406004; 226689508 00763000624767; 226711355 00763000406004; 226711356 00763000406004; 226711357 00763000406004; 226738254 00763000406004; 226738255 00763000406004; 226738256 00763000406004; 226738257 00763000406004; 226899374 00613994445360; 227136767 00763000624767; 227136768 00763000624767; 227136769 00763000624767; 227187464 00763000624767; 227187465 00763000624767; 227188106 00763000624767; 227194730 00763000624767; 227289113 00763000406004; 227289114 00763000406004 22728911500763000406004— - Amount recalled
- 30,711 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.
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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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