FDAJuly 23, 2021device

TheraSphere Administration Set, REF OTT-SPE-FP-001 (990264.SPE)

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

The hazard

Potential for leaks and loosening at the patient catheter connection

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

05060116920635

Recall history

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

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