FDADecember 4, 2019device

0.035"(.89mm)x150 cm guidewire. Model 114135150. Soft Tip 3.5cm. REF/UDI: 114135150/(01)20886333008074. RxOnly.STERILE EO

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

The hazard

The stiffness of the soft end of the guidewire caused tissue perforation.

What to do

FDA enforcement status: Terminated

Brands named

argon medical devicesargonargon medical

UPCs

20886333008074

Recall history

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

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