FDASeptember 12, 2025device

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava (IVC) in the following conditions: " Pulmonary thromboembolism when ant...

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

The hazard

Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied

What to do

FDA enforcement status: Ongoing

Brands named

argon medical devicesargonargon medical

UPCs

00886333217151

Recall history

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

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