FDASeptember 14, 2020device

Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media Ref: P6153208

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

The hazard

Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

UPCs

00801741141065

Recall history

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

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