FDAMarch 5, 2024device

OptiCross Coronary Imaging Catheter, REF H749518080120

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

The hazard

Certain batches of Opticross 40MHz Coronary Imaging Catheters manufactured using an incorrect voltage setting, which may have resulted in decreased image brightness.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

08714729938415

Recall history

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

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OptiCross Coronary Imaging Catheter, REF H749518080120 — Recall Details · AllClear