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FDAFebruary 17, 2016device

Catheter, Intravascular, Therapeutic, Short-Term Less than 30 days The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access.

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

The hazard

Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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