FDAOctober 24, 2019device

Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide. Packaged in the following sizes: 1. REF/Catalog No. H7493933515060, 6F; 2. REF/Catalog No H7493933515070, 7F.

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

The hazard

Certain dilation and extension catheters are being recalled because these catheters may have missed the hydrophilic coating step, which creates a lubricious surface on the devices, during the manufacturing process.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

UPCs

87147299394508714729939474

Recall history

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

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