FDASeptember 17, 2018device

Reprocessed Agilis Steerable Introducer: indicated for introducing various cardiovascular catheters into the heart. (a) small curl (16.8mm curve type/71 cm length), Product Code STJ408309; (b) medium curl (22.4 mm curve type/71 cm length), Product Code STJ408310; (c) large curl (50 mm curve type/...

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

The hazard

Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements per product specification for biological residues determined by LAL testing.

What to do

FDA enforcement status: Terminated

Brands named

sterilmed

UPCs

108885510449121088855104492910888551044950

Recall history

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

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