FDAMarch 1, 2019device

BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536

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

The hazard

Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

UPCs

382903835362

Recall history

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

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