FDAOctober 23, 2020device

Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully Articulating Catheter within the lung to a planned path in order to sample a target. User Manual: ION Endoluminal System, System, Instruments, and Accessories User Manual, PN 553990-05 R...

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

The hazard

The distal tip ring of the fully articulating catheter may become dislodged during the procedure.

What to do

FDA enforcement status: Terminated

Brands named

intuitive surgicalintuitive

UPCs

00886874116258

Recall history

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

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