FDAMarch 8, 2024device

Route 92 Medical Full Length 070 Access System, REF 7002, Rxonly, SterileEO. Used for Introduction of interventional devices into the neurovasculature.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Their is the potential for distal tip separation at the proximal marker band of the delivery catheters.

What to do

FDA enforcement status: Ongoing

Brands named

route 92 medicalrouteroute 92

UPCs

00853799007473

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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